paid research studies in la

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Clinical Trials in Los Angeles, California

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Los angeles, california.

Los Angeles, the "City of Angels" is California's largest city and is second only to New York in population. It is known for the Hollywood entertainment industry, mild climate, bumper-to-bumper traffic, ethnic diversity and considerable leisure and outdoor opportunities. When it comes to health care, this sprawling metropolis has more than 25 hospitals with scores more in the surrounding Los Angeles county. So, there is no shortage facilities for Angelenos to receive general medical services, emergency and acute care, and specialty health care.

Below are some of the best hospitals in the city of Los Angeles, according to U.S. News and World Report. The media company's Best Hospitals rankings helps consumers make decisions about where to find inpatient hospital care in their community and beyond. Los Angeles clinical trials can be found at almost all of them.

UCLA Health

For more than 30 years, the UCLA Health system has been ranked among the country's best in U.S News and World Report's annual review. Within the LA city limits, three UCLA hospitals reside on the UCLA Health main campus in the Westwood section of the city. Ronald Reagan UCLA Medical Center, UCLA Mattel Children's Hospital and UCLA Resnick Neuropsychiatric Hospital:

Ronald Reagan UCLA Medical Center

With more than 1,500 doctors on staff, Ronald Reagan UCLA Medical Center cares for more than 300,000 people a year from greater Los Angeles, California and around the world. It is a general medical and surgical hospital, level one trauma center and teaching facility. US News and World Report has ranked it as the 4th best hospital in the U.S. and first on the West Coast.

UCLA Mattel Children's Hospital

Located on distinct floors of the Ronald Reagan UCLA Medical Center, UCLA Mattel Children's Hospital attracts pediatric patients from all over California. Physicians provide the full range of general and specialty care to infants, children, adolescents, and young adults up to age 21. The hospital has ranked nationally in all pediatric specialties reviewed by U.S. News & World Report.

UCLA Resnick Neuropsychiatric Hospital

Residing on a floor of the Ronald Reagan UCLA Medical Center, UCLA Resnick Neuropsychiatric Hospital provides world-class patient care to adults and children in the areas of mental health, developmental disabilities, and neurology. The hospital's many programs include treatment for ADHD, eating disorders, anxiety, and sleep disorders.

Children's Hospital of Los Angeles

Children's Hospital of Los Angeles opened in 1901 in a small house in what is today's Chinatown. Over the years, it has grown to include more than 350 pediatric specialty programs and services. The hospital's Heart Institute has gained world-wide recognition for treatment of heart and lung disorders in children and has one of the busiest cardiac care programs in the nation. U.S. News and World Report has ranked this institution among the top five children's hospitals in the country.

Cedars-Sinai Medical Center

Often regarded as the hospital of Hollywood celebrities, Cedars-Sinai Hospital had humble beginnings in 1902 as a 12-bed hospital. Today, it is the largest non-profit hospital in the country with 4,500 physicians and nurses and nearly 900 beds. U.S. News and World Report has ranked Cedars Sinai #7 in its authoritative review of Best Hospitals. Boasting a robust medical research program, the hospital offers extensive array of clinical trials in Los Angeles. It has one of the largest, most advanced research facilities of any private hospital in the country.

Keck Hospital of USC

Keck Hospital of USC, east of downtown Los Angeles is an acute care hospital with just over 400 beds. Hundreds of clinical trials in LA taking place at Keck Hospital and its affiliated institutions, offering participants access to potential therapies that are not yet widely available. The hospital has ranked #18 nationally on U.S. News and World Report's Best Hospitals honor roll.

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Paid Clinical Trials in Los Angeles, CA

Find paid studies that are recruiting healthy participants in Los Angeles, CA. Filter by distance, duration, and inclusion criteria to find clinical trials that pay well for your time.

Here are the 6 most popular medical studies in paid studies los angeles

Michael Bask Gill, B Sc

Last Reviewed: March 15th, 2024

Dietary Supplement

Radicle gi health active study product 1.1 for abdominal pain, this trial will test how health and wellness products affect gut health and overall health outcomes in a fair and unbiased manner..

JK07 for Heart Failure

"this trial is testing a new drug, jk07, on adults aged 18-85 with heart failure. the study will have two groups of participants based on the strength of their heart. participants will.

Neonates with hyperinsulinism for Hyperinsulinemia

The investigators are studying the accuracy of dexcom g6 continuous glucose monitors placed on babies with hyperinsulinism in the miller children's hospital neonatal intensive care unit. the participants will wear the device for 10 days on their lateral thigh. whenever blood sugars are checked by glucometer, the investigators will also record the continuous glucose monitor sugar. additionally, if the continuous glucose monitor alarms for a low sugar or an impending low sugar, the investigators will check the blood sugar by glucometer and, if verified to be low, treat the low blood sugar accordingly..

Stem Cell Therapy

Wharton's jelly allograft for lower back pain, "this trial is a small preliminary study where 100 people with low back pain will receive wharton's jelly allograft to see if it is safe and possible to use.".

SNOO users for Sudden Infant Death Syndrome

This postmarket surveillance study will evaluate the safety of the snoo smart sleeper bassinet when used for infants who are at high risk for sudden unexpected infant death (suid). this study will survey 1000 caregivers of high-risk infants to examine the frequency of death or serious injury occurring in the snoo bassinet..

Behavioral Intervention

Who is luke eemia for leukemia, this trial aims to see if using a storybook along with the standard child life intervention can reduce stress in parents of children diagnosed with leukemia. they will compare the stress levels of parents who receive the story, popular filter options for paid studies los angeles trials, phase 3 clinical trials.

View 96 phase 3 medical studies.

Behavioural Intervention

Lumateperone for depression, bipolar disorder, "this trial is studying the effectiveness of a new treatment for children with bipolar disorder who are also experiencing major depressive episodes. the study is being conducted at multiple locations and will involve random assignment of participants to receive.

Iron Supplement

Venofer +1 more for iron-deficiency anemia, this trial aims to see if giving pregnant women with low iron levels intravenous iron early in pregnancy is better than the standard oral iron treatment. women with low iron levels were randomly given either oral or intr.

Histamine H3 Receptor Antagonist

Pitolisant for prader-willi syndrome, this trial is testing a medication called pitolisant to see if it can help patients with prader-willi syndrome who experience excessive daytime sleepiness. the study will also look at how pitolis.

Solriamfetol for Depression

This trial, called paradigm, is testing a drug called solriamfetol to see if it is safe and effective in treating major depressive disorder in adults..

Fasedienol Nasal Spray for Social Anxiety Disorder

"this trial will test the effectiveness, safety, and tolerance of a nasal spray called fasedienol in reducing anxiety symptoms in adults aged 18-65 with social anxiety disorder. the study will also.

Alpha Blocker

Phentolamine ophthalmic solution for night vision, this trial tests if using a specific eye drop can help people who have vision problems after eye surgery., clinical trials with no placebo.

View 96 medical studies that do not have a placebo group.

Observational for Breast Cancer

This study evaluates the side effects and outcomes of patients who undergo cryoablation for early stage breast cancer..

Intrahepatic Cholangiocarcinoma, With Lymph node metastasis (Validation) for Bile Duct Cancer

Lymph node metastasis (lnm) is a major prognostic factor in intrahepatic cholangiocarcinoma (icc), and accurate preoperative prediction of the presence or absence of lnm has significant clinical implications in determining treatment strategy. despite this, there are currently no reliable biomarkers established to detect lnm in icc. this study seeks to develop a liquid biopsy assay that can accurately detect lnm before treatment in icc patients..

Patients with Esophageal Adenocarcinoma or High-Grade Dysplasia Barrett's Esophagus [Validation] for Barrett's Esophagus

This study aims to develop a highly sensitive, specific, and cost-effective blood assay for the early detection of esophageal adenocarcinoma and its precursor lesions, using advanced machine learning and state-of-the-art biological analyses..

Irrisept Irrigation +1 More for Acne

This trial aims to see if there is a difference in the presence of a type of bacteria called c acnes in samples taken from different depths of tissue before surgery. the participants will receive either normal sal.

Narrative Medicine for Gastrointestinal Cancer

This trial aims to see if using storytelling methods, known as narrative medicine, can help improve the emotional well-being of patients with gi cancer. narrative medicine involves healthcare providers listening to patients' stories about their.

Download the REMAIN App for Human Immunodeficiency Virus Infection

Despite the widespread availability of effective antiretroviral therapy (art) in the united states, there remains significant numbers of people living with hiv (plwh) who fail to achieve and or maintain viral suppression (vs). disparities persist with the lowest levels of vs among black individuals, people who use drugs, youth ages 18-24 and people residing in rural areas. investigators will examine the syndemics underlying these outcomes including substance use, mental health, and barriers to hiv care including racial discrimination, stigma and rural isolation., paid clinical trials.

View 96 medical studies that offer remuneration.

AZD0233 for Dilated Cardiomyopathy

"this trial aims to test the safety, side effects, and how the body processes azd0233 in healthy volunteers after receiving different doses of the medication.".

Monoclonal Antibodies

Sr604 for healthy subjects, this trial will test a new medication called sr604 in two groups of people. the first group will be healthy individuals to see how safe the medication is and how the body processes it. the second group.

Ultradent Ultra Seal XT Plus for Sealant

This trial aims to compare the longevity of sealants with a bonding agent cured before placement versus those with an uncured bond in pediatric dental patients. the study will be conducted by usc graduate pediatric personnel at, ecc5004 for type 2 diabetes, "this trial is looking at how ecc5004 affects the levels of certain medications (atorvastatin, rosuvastatin, digoxin, and midazolam) in healthy participants.

PF-06954522 for Type 2 Diabetes

"this trial aims to test the safety and effectiveness of different doses of pf-06954522 in adults with type 2 diabetes who are already taking metformin. it will also include non-diabetic.

Local Anesthetic

Exparel for pain, this trial aims to see if a specific type of pain medication called exparel can help reduce the amount of narcotic pain medication needed after acl surgery in teenagers., view more paid studies los angeles trials.

See another 72 medical studies focused on paid studies los angeles.

Estring Vaginal Product +2 More

Heart rate variability biofeedback

Advanced Adenoma (Training cohort)

Patients with Gastric Cancer (Training)

Hepatocellular Carcinoma (Validation)

Early onset colorectal cancer (Validation cohort)

Insulin glargine +1 More

Bladder Transplantation +1 More

Bictegravir +1 More

Observational (survey, biospecimen, medical record, CT)

NNC0519-0130

Semaglutide +1 More

Cagrilintide

T1 Colorectal Cancer, Without Recurrence (Training)

Stage II/III Colorectal Cancer, without Recurrence (Training)

Zirconia Implants

Parent-Child Interaction Therapy (PCIT)

Epidural electrical spinal cord stimulator

Fasting +1 More

Retatrutide

Hip-Hop Dance

Savoring Intervention

Lepodisiran

Ravulizumab

GS-1427 +1 More

Air up® Drinking System

Normal Cognition (NC) with at least 1 vascular risk factor

Budesonide +1 More

ColActive Plus Collagen Matrix Dressing

Brace With Electrical Diodes

TMS Stimulation

Positive Affect Treatment

SteadiSet Extended Wear Infusion Set

Skin Prick Test

Survivors of early-onset colorectal cancer, with recurrent disease (Training Cohort)

IcoSema +1 More

Baxdrostat/dapagliflozin

Fixed Sequence 2

NBI-1070770

Atezolizumab +1 More

Partners - MGH/BWH

NNC6019-0001

Virtual Reality (VR)

UC-A +1 More

Continuous Glucose Monitor

View more paid studies los angeles

See more medical studies focusing on paid studies los angeles

Frequently Asked Questions

Other Trials to Consider

High-Stress Intervention

Formulation a (reference) followed by formulation b (test), prolonged exposure, healthy lifestyle behavioral intervention (mbs -supported intervention), increasing willingness and uptake of covid-19 vaccination, high-frequency (hf), extension for community healthcare outcomes, acupuncture therapy, mobile contingency management, free light chains, standard behavioral treatment plus relationship skills training, multi-level preschool obesity control intervention, healthy together (includes streetwyze) (control/standardized care), popular categories.

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Clinical Trials in Ventura, CA

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Paid Clinical Trials in Baltimore, MD

Paid Clinical Trials in San Diego, CA

Paid Clinical Trials in San Francisco, CA

Paid Clinical Trials in Sacramento, CA

Paid Clinical Trials in Tucson, AZ

Paid Clinical Trials in Anaheim, CA

Paid Clinical Trials in Long Beach, CA

Paid Clinical Trials in Ventura, CA

Paid Clinical Trials in Georgia

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Paid Clinical Trials in Rhode Island

Popular guides.

Call to join a study

The recognized leader in clinical trials resulting in new and better medicines.

Active studies, generalized anxiety study (gad).

Age 18-65 · Male / Female

Compensation TBD

Attention Deficit Hyperactivity Disor...

CenExel CNR is seeking volunteers living with ADHD to participate in our clinical trial.

Age 18-55 · Male / Female

Free Memory Evaluation

Age 50+ · Male / Female

At Risk for Alzheimer’s Disease Study

Age 60-80 · Male / Female

Compensation up to $5,500

Obsessive Compulsive Disorder (OCD) T...

We're studying an investigational drug to potentially help treat the symptoms of OCD.

Compensation up to $675

Migraine Trials

Still struggling to manage migraines? Don't settle.

Age 18 and up · Male / Female

Compensation up to $1,725

Major Depression Trials

Age 18-74 · Male / Female

Compensation up to $1,000

Memory Loss Study

Age 55-85 · Male / Female

Don’t see what you’re looking for? Simply complete this  information form , and we’ll find a study that fits you.

Read about our COVID-19 safety precautions

Accelerate healthcare

Help in development of future medicines.

Your participation will be incredibly valuable in providing researchers with information to move forward, regardless of the outcome of the clinical trial.

Gain access to new medical treatments

California Neuroscience Research offers participants innovative medicines at the leading edge of pharmaceutical evolution.

Receive compensation for time & travel

While the financial benefits of participation typically won’t replace the need for a regular job, you will be paid for your time and travel expenses.

Clinical research provides first-class medical care

Every study at CenExel CNR is overseen by expert medical staff and one of the most well-respected, board-certified physicians in the clinical research industry.

25+ years of clinical trial experience

WELCOME TO SANTA MONICA CLINICAL TRIALS

Santa Monica Clinical Trials is a private clinical research site located in Los Angeles, California. Our Investigators have over 20 years of experience and are engaged in numerous phase II-IV clinical research trials, including drug and medical device studies. Participation does not require proof of medical insurance. All trials are conducted under FDA guidance and regulations.

If you or a loved one suffers from one of these disorders, take the next step and contact a member of our study team today!  No medical insurance needed. Compensation for time & travel may be available.

Current trials, motion sickness.

Motion sickness is a common condition affecting about 30% of the population. Common symptoms of motion sickness include nausea, vomiting, stomach awareness, pallor, headache, sweating, dizziness, a sensation of warmth and drowsiness. The purpose of the study is to evaluate the effectiveness of an investigational drug on symptoms associated with motion sickness and to assess the safety of the investigational drug.

SLEEP DISTURBANCES IN INDIVIDUALS WITH AUTISM SPECTRUM DISORDER

Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder that is associated with persistent deficits in social communication, restricted/repetitive behaviors, among other symptoms. Sleep disruption in individuals with ASD is higher than in healthy controls with a documented prevalence of up to 80%. The purpose of this study is to evaluate the effectiveness and safety of the study medication on sleep in individuals with autism spectrum disorder.

DELAYED SLEEP-WAKE PHASE DISORDER

Delayed sleep–wake phase disorder (DSWPD) is a chronic dysregulation of a person's circadian rhythm (biological clock), compared to those of the general population and societal norms.  People with DSWPD generally fall asleep some hours after midnight and have difficulty waking up in the morning. However, they find it very difficult to wake up in time for a typical school or work day. If they are allowed to follow their own schedules, e.g. sleeping from 4:00 am to 1:00 pm, their sleep is improved and they may not experience excessive daytime sleepiness. The purpose of this study is to evaluate the efficacy and safety of an investigational medication compared to placebo for this condition.

SLEEP APNEA

Obstructive Sleep Apnea (OSA) is a common and serious sleep disorder in which breathing is repeatedly interrupted during sleep. OSA occurs when the airway collapses as you breathe in. This can cause breathing to be paused from several seconds to over a minute. 

While many people use continuous positive airway pressure (CPAP) machines to manage their OSA, these systems can be cumbersome and awkward for some. The LunAIRo study involves an investigational oral medication for people who have OSA. The investigational medication will be taken daily at bedtime. 

ARE YOU ELIGIBLE?

If you’re interested in participating in one of our current or upcoming studies, please contact our office today to inquire about your candidacy.

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We bring tomorrow’s medicines to you today, volunteer enrollment is underway for our clinical trials. call today to see if you qualify.

Our Clinical Research Studies Are Designed For You

The list below is just some of the studies that we are currently enrolling. If you have any of these conditions and want to earn compensation and help bring tomorrow’s medicines to people then don’t wait call us today:

• Alzheimer Disease
• Atherosclerotic Cardiovascular Disease
• Cytomegalovirus (CMV) Vaccine
• History of Major Adverse Cardiovascular Events
• Hyperlipidemia
• Hyperlipoproteinemia
• Interstitial Cystitis (Bladder Pain)
• Non-Muscular Invasive Bladder Cancer
• Overactive Bladder
• Urinary Tract Infection Vaccine

Volunteering is Fast, Confidential, and Worthwhile!

Our caring staff of medical professionals will be with you every step of the way, from qualifying to completing your trial. Our studies are designed for your convenience and to help you with your condition all at no charge to you. You get these significant benefits:

• Free medical evaluation and health exam
• Free lab analyses and reports
• Free advanced, study-related investigational medicines
• Guaranteed monetary compensation
• Free transportation or reimbursement for travel
• HIPAA-compliant
• Fully private and confidential
• Choice of different FDA-governed studies
• All medical safety standards are followed

How It Works

If you or a loved one has one of the conditions that we currently enrolling for, follow these 5 simple steps to get tomorrow’s medicines today:

Fill out the simple form below

You will be contacted by one of our professional study screeners., the screener will schedule a free medical consultation and exam based on the study., your study appointments will be set, and medication will be dispensed., you get paid, it’s just this simple and you do not need medical insurance or proof of residency to participate..

American Institute of Research in downtown Los Angeles is here to bring you advanced medicines and hope for future sufferers. By participating in a clinical trial you are helping yourself with exciting new investigational medications in various trial phases. Trials such as these have led to the world’s better health and cures for some of the most devastating of diseases, just imagine being part of a team that helps discover a new medication that dramatically improves your condition all while being compensated for your involvement. That is a win-win.  

Our lead investigators are some of the most respected doctors in Los Angeles. They are an integral part of the Los Angeles medical community. Each investigator is a specialist in the area of the particular study that you qualify for and they have been at the research front helping people such as you for years with their conditions. This means that you will not only be getting tomorrow’s medicines today but you will also be monitored by some of the best physicians in their fields in Los Angeles.

Call Today or fill out the form below and get started.

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Our Mission

Altasciences conducts contract clinical research to assess the safety and effectiveness of new medications. We are always recruiting participants to take part in clinical studies. We are interested in healthy adult participants, as well as those with a specific illness or medical condition depending on the needs of each trial.

We are committed to your safety and comfort during our trials.

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Altasciences has clinics in both the U.S. and Canada, where experienced medical and clinical professionals oversee all aspects of trial conduct. Click on your location to see the open trials we are recruiting for:

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HOPE STARTS HERE

Begin your journey to better health and wellness through our paid clinical trials in the greater Los Angeles area.

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Unlock the Potential of Medical Research

Paid clinical trials help you find relief through exciting medical advancements. Volunteering allows you to try new treatments, procedures, and devices you won’t find anywhere else. It's a safe and effective way to discover new healthcare options and feel better!

Be a Part of Something Bigger

At our medical research clinics in Los Angeles, patients have embarked on the same journey of hope and transformation. With your participation, finding answers is possible and helps millions of people with the chance of curing lifelong diseases in the future.

Finally, Get the Treatment You Deserve

With the support of our expert medical team, you can take charge of your well-being and embrace a brighter outlook. If you're looking for a medical setting where you feel valued and see results , we invite you to join one of our studies.

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THE HIGHEST-PAYING CLINICAL TRIALS YOU CAN PARTICIPATE IN

Discover top-paying clinical trials in your area. Our guide highlights the most common and accessible trials.

THE TOP 5 SKILLS EVERY CLINICAL RESEARCH ASSOCIATE OR COORDINATOR SHOULD HAVE

These five skills for top-performing CRAs or CRCs are a must for the success of new medical treatments.

THE IMPORTANCE OF CLINICAL RESEARCH IN ADVANCING MEDICINE

Make a difference and improve your health! Discover why paid clinical research studies are so important for medicine.

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• Flu Symptoms Study

818-296-6983

Join a clinical research study and earn up to $7,000, sign up today – space is limited, clinical study enrollment is open now.

Now you have an opportunity to explore improved treatment options and also earn extra money participating in an FDA-governed clinical research study. It’s easy…it’s convenient…and enrollment is open to you right now.

CALL 818-296-6983 TO FIND OUT IF YOU QUALIFY

Featured clinical studies, click on study name to learn more and join, join our current studies, join a paid fda clinical research study in canoga park…, you’re needed for an fda-approved clinical study – with pay, earn up to $7,000.

Are you suffering from a troubling health condition? If so, you have an opportunity to explore improved treatment options and also earn extra money participating in an FDA-licensed and approved clinical research study. It’s easy…it’s convenient…and it’s open to you right now.

Sign Up for a Clinical Research Study Today

We are conducting many studies at this time. View CURRENT STUDIES in the menu above. Contact us to participate in a current study or be notified of upcoming studies. Study space is limited.

HERE IS HOW TO GET STARTED

As a study participant, you play a valuable role in helping to get safe, effective drugs approved for public use. Because you are such an important part of our studies, we have simplified the steps for participation.

Call Toll-Free 1-818-296-6983 or Click on a Study Below

This is the first step. All volunteers will be able to review the Informed Consent form, and the program will be carefully explained by our professional medical team.

Come in for a FREE Medical Exam

After evaluating your particular medical situation, we will invite you into our clinic for a comprehensive and complimentary physical exam.

No Special Requirements

If you meet the physical guidelines of the study, you will be asked to participate. No medical insurance is needed to participate.

Receive Up to $7,000

Participants will be assigned to different groups, where you will be carefully monitored for treatment and safety. As a volunteer, you will earn as much as $7,000.

Want to Join a Paid Study?

Choose one that fits you. All volunteers will be able to review the Informed Consent form, and the program will be carefully explained by our professional medical team.

WHAT YOU SHOULD KNOW

This professional clinical study, conducted by Clinical Research LA, is a short term trial in which you will intake a promising new medication seeking FDA approval. Depending on the study you join, this medication’s use is intended to effectively treat your medical condition. Here is what you can expect, regarding these studies:

• Complimentary consultation and health exam
• Complimentary comprehensive lab reports
• Complimentary study-related medicines
• Studies for diabetes, osteoarthritis, asthma, others
• Meets all industry safety guidelines
• Governed & monitored by the central ethics committee
• You will be compensated for your time and travel
• FDA-approved
• HIPAA-compliant
• Full confidentiality
• Guaranteed monetary compensation
• Your participation will help provide data on the effectiveness of the vaccine

Clinical Research LA

A respected medical team.

Our clinical research clinic has extensive experience conducting Phase II through IV clinical trials with many leading pharmaceutical companies. The facility features multiple investigators with many years in clinical research and counts over 10,000 patients. Every member of the team offers a wealth of experience, a caring personality and a commitment to ably serving the pharmaceutical industry, the community, and its patients.

Our team of clinical research investigators brings many years of research experience working at UCLA and USC. They speak English, Spanish, Italian and Farsi.

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PAID STUDIES IN LOS ANGELES

L&E Opinions offers remote and in-person access to hundreds of research studies, product testing, and focus panels. Getting paid to participate is easy!

The sign-up process for studies in Los Angeles is easy

Join the l&e community.

Create your free account and fill in your profile

Browse studies and submit your profile for those that suite you

Complete the study and get paid

Discover the types of studies we offer in Los Angeles

Research studies.

Some studies might involve simple tasks like completing a survey, being observed among a group of people or participating in a group discussion.

Focus Groups

Focus groups in Los Angeles are interviews involving a small number of demographically similar participants who have other common traits and/or experiences. We study reactions to specific researcher/evaluator-posed questions and use that information to help our clients make important business decisions.

Product Testing

L&E Opinions also performs Product testing for our Los Angeles clients. Product testing is sometimes referred to as consumer testing or comparative testing. Our goal is to measure the properties or performance of a certain product and report those results to our clients.

L&E Research conducts three formats of market research projects in Los Angeles:

In-person research.

where you come in to our offices or another location to take part in the research

Telephone surveys

that you take when we call you on your landline or cell phone

Online surveys

that you take on your computer, tablet or smartphone

If you would like more information about the process of signing up, participating, and getting paid, learn how it works .

READY TO GET PAID FOR YOUR OPINIONS?

• Dr. Shahram Jacobs
• Hospital Access

Pediatric Psoriasis

Atopic dermatitis.

• Chronic Kidney Disease/Anemia
• Tinea Pedis (Foot Fungus)
• Upcoming Trials

Physician Referral

• Join Patient Database

PAID CLINICAL TRIALS IN LA

Safe. no out-of- pocket cost..

• No medical insurance needed
• Compensation for participation
• FDA-supervised trials

We are committed to assessing the safety and effectiveness of the latest drugs, medications, and treatments that promise optimal health outcomes for individuals who are diagnosed with chronic diseases. In this way, we provide our Los Angeles patients with progressive care that may deliver profound and lasting relief from their conditions.

Evaluating cutting-edge treatment approaches. Delivering innovative care to patients who need it most.

Tinea Pedis

Also known as athlete’s foot, tinea pedis causes fungus to grow on the feet. Although it is not a serious condition, it results in uncomfortable itching, discolored toenails, peeling skin and more. This clinical trial aims to test the efficacy of a topical medication for this condition.

Chronic Kidney Disease / Anemia

Chronic kidney disease (CKD) is a serious condition that affects approximately 30 million adults in the U.S. and can lead to total kidney failure. Designed for patients with CKD stages 3, 4, or 5, this clinical trial will evaluate the efficacy of oral or injectable medications.

Adult Psoriasis

Adult psoriasis is a skin condition that is characterized by itchy patches and silvery scales. There is no cure, and the disease tends to flare-up in response to outside factors, such as stress, trauma, and certain infections. We are currently holding two adult psoriasis studies to test the efficacy of a topical medication and an injectable biologic medication.

Atopic dermatitis, also referred to as eczema, is a chronic skin condition characterized by itchy and inflamed skin rashes. It can occur at any age, though it is more common in children.

Pediatric psoriasis is a chronic, incurable skin condition that causes itchy, red areas and scales. It affects approximately 1% of children in the U.S. At Unison, we are currently recruiting participants for a new clinical trial evaluating a topical lotion/foam for managing the symptoms of pediatric psoriasis in healthy children.

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Upcoming Clinical Trials

Our research team at Unison is excited to announce several new and exciting clinical trials on the horizon – including studies for arthritis, rosacea, irritable bowel syndrome-diarrhea, irritable bowel syndrome-constipation, diabetes, acne, and more.

If you’re interested in participating in one of our upcoming studies, please contact our practice today to see if you qualify.

Are you Eligible?

If you're interested in participating in one of our upcoming clinical trials, please join our patient database today. After reviewing your information, we will contact you to schedule a consultation if you qualify for a study.

Join Our Database >>

Our providers.

The board-certified providers which form the team at Unison Clinical Trials are committed to the comfort and safety of all clinical trial participants. All of our team members possess the knowledge, training, and volumes of experience necessary for successful clinical research in Los Angeles.

The Unison Clinical Trials team has been working in real-world clinical research environments for several years (over a decade). Thousands of patients have enrolled in paid clinical trials in California led by these highly experienced professionals, and many more can be found on our rosters today.

Individually, each Unison team member possesses extensive certification, licensing and knowledge, and a commitment to the health of their community and the advancement of the field of medical science. Together, they provide incredible value and insight into some of today’s most pressing medical conditions.

Administering the most advanced medical care available, our team can conduct clinical trials in Los Angeles for study participants who receive treatment for their medical conditions. We offer the most advanced products from pharmaceutical companies at no cost. Because our team is so vitally important to us, we ensure that measures to protect their safety are always in place.

The Unison Clinical Trials team is led by Dr. Shahram Jacobs, an award-winning physician who possesses extensive experience in the implementation of clinical trials.

Patient Care

At Unison Clinical Trials, our top priority continues to be the delivery of excellent patient care. Our team employs efficient procedures and takes every available precaution while participants undergo treatment with trial medications.

When you enroll in one of our paid medical studies in Los Angeles you’ll not only receive the latest treatment for your condition, but you will also be closely monitored with various lab and diagnostic procedures throughout the study.

Our Facilities

We strive to create a safe and welcoming environment for all California clinical trial study participants. In addition to featuring a soothing energy, our high-tech research center facilities are fully equipped with the latest technology that enables us to monitor you closely throughout the study, perform all diagnostic tests as necessary, and ensure that your health is protected.

Our trial participants benefit from access to an EKG machine, laboratory, and ultrasound machine on site. We also offer convenient off-site access to x-rays and specialty services such as sleep labs and blood pressure monitoring...

Unison is located in beautiful Sherman Oaks, California. Our past and current medical participants come from Los Angeles, Santa Barbara, Orange County, northern California, and even out of state. If you have been trying to manage your condition without success, you may be able to get the treatment and care you need, and receive payment for participating in a clinical trial at Unison.

We are in the process of actively recruiting volunteers from Southern California looking to participate in paid medical research by enrolling in one of our clinical trials. Many opportunities to participate in our clinical trials exist; if you’re ready to explore the clinical research studies at our medical center, simply access the menu at the top right.

We strive to create a safe and welcoming environment for our clinical trial participants. In addition to featuring a soothing energy, our high-tech facilities are fully equipped with the latest technology that enables us to monitor you closely throughout the study, perform all diagnostic tests as necessary and ensure that your health is protected.

“You can be assured that you are receiving access to the very best medical care.”

- Shahram Jacobs, M.D.

Physician referrals are an integral part in finding clinical trial participants. We believe in a straightforward referral process to efficiently match qualified patients with cutting-edge treatments, and strive to cultivate a collaborative relationship with patients’ primary healthcare providers for optimal quality of care and communication.

© Unison Clinical Trials. All rights reserved. Designed & Developed by Studio III

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Find a Trial

Clinical trials in los angeles, ca.

Are you looking for a clinical trial in Los Angeles, California? The City of Angels is able to conduct important studies like " Reduced Craniospinal Radiation Therapy and Chemotherapy in Treating Younger Patients With Newly Diagnosed WNT-Driven Medulloblastoma " and " Study to Evaluate Safety and Efficacy of Dapagliflozin in Patients With Type 2 Diabetes Mellitus Aged 10-24 Years " thanks to it’s diverse patient population and industry-leading clinical trial facilities.

While some individuals are looking for paid research studies in Los Angeles, others want to help experts in the fields of oncology and rheumatology develop better treatments for chronic illnesses. Ready to start? Complete the form to the right to find new Los Angeles clinical trials that are close to where you live.

Use our guide to learn which trials are right for you!

We've found 2,654 clinical trials in california.

Select your condition

Common conditions.

• Atrial Fibrillation
• Breast Cancer
• Constipation
• Dermatology
• Fibromyalgia
• Healthy Studies
• High Blood Pressure (Hypertension)
• High Cholesterol
• Irritable Bowel Syndrome (IBS)
• Migraine Headaches
• Obesity Weight Loss
• Osteoarthritis (OA)
• Renal Impairment / Chronic Kidney Disease
• Skin Cancer
• Smoking Cessation

All Conditions

• Alzheimer Disease
• Athletes Foot
• Benign Prostate Hyperplasia
• Bipolar Disorder
• Bladder Cancer
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• Cognitive Studies
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• Contraception Birth Control
• Contraception Birth Control Patch
• Crohns Disease
• Diabetic Neuropathy
• Digestive Disease
• Diverticulitis
• Eating Disorder
• Endometrial Cancer
• Endometriosis
• Erectile Dysfunction
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• Hepatitis C
• Infectious Disease
• Infertility
• Influenza Vaccine
• Insomnia Sleep Studies
• Iron Deficiency Anemia
• Kidney Cancer
• Liver Cancer
• Low Back Pain/Arthritis Pain
• Lung Cancer
• Major Depression Disorder (MDD)
• Menses Disorders
• Multiple Sclerosis
• Osteoporosis
• Other Indications
• Ovarian Cancer
• Overactive Bladder
• Pancreatic Cancer
• Parkinsons Disease
• Peripheral Vascular Disease
• Polycythemia Vera
• Post-Surgical Pain
• Postherpatic Neuralgia
• Postmenopausal Syndrome
• Premature Ejaculation
• Prostate Cancer
• Psychiatric
• Restless Leg Syndrome
• Rheumatoid Arthritis
• Rheumatology
• Schizophrenia
• Shingles Vaccine
• Skin and Soft Tissue Infections
• Thyroid Cancer
• Tobacco Consumers
• Tobacco Consumers: SNUS, Chew, Dip
• Urinary Tract Infections
• Women's Studies

(504) 934-8424

(985) 219-6501

(504) 934-8092

(985) 302-0470

(646) 386-7574

(407) 636-4031

(732) 724-2500

(407) 680-0534

Tandem Clinical Research Is a Dedicated Phase I-IV Clinical Trials Network

We specialize in the performance of clinical trials for pharmaceutical, biotech, and medical device companies. All medical service is provided free of charge by board-certified physicians. Click an image below to learn more.

How Does It Work?

What to Expect?

Benefits of Participating

How do clinical trials work.

Clinical trials are a crucial part of clinical research that test new medical treatments, drugs, or interventions on human participants to determine their safety and effectiveness. Here’s how they work:

• Study Design: Before a clinical trial begins, researchers carefully plan and design the study. They define the objectives, eligibility criteria for participants, and the treatment plan. This design ensures that the trial produces reliable and meaningful results.
• Phases of Clinical Trials: Clinical trials are typically conducted in multiple phases: a. Phase 1: These trials involve a small number of healthy volunteers to assess the treatment’s safety, dosage, and potential side effects. b. Phase 2: In this stage, the treatment is given to a larger group of patients who have the specific condition the treatment aims to address. Researchers monitor its effectiveness and further evaluate its safety. c. Phase 3: The treatment is tested on an even larger group of patients to compare its effectiveness against existing standard treatments or placebos. This phase provides more comprehensive data on safety and efficacy. d. Phase 4: After the treatment receives regulatory approval, Phase 4 trials are conducted to monitor its long-term safety and effectiveness in a broader population.
• Randomization: Participants are randomly assigned to different groups. For example, in a Phase 3 trial, some participants might receive the new treatment while others receive the standard treatment or a placebo. This randomization helps minimize bias and ensures fair comparisons.
• Blinding (Masking): Blinding means that participants and/or researchers may not know which treatment each participant is receiving. This prevents bias and helps obtain more objective results. Trials can be single-blind (participants don’t know), double-blind (neither participants nor researchers know), or open-label (both know).
• Informed Consent: Before joining a clinical trial, participants must receive detailed information about the study, including potential risks and benefits. They give their informed consent to participate voluntarily.
• Monitoring and Data Collection: Throughout the trial, researchers closely monitor participants’ health and collect data on their responses to the treatment. This includes regular check-ups, tests, and questionnaires.
• Analysis and Results: After the trial is completed, researchers analyze the data to determine the treatment’s effectiveness and safety. The results are usually published in scientific journals, contributing to medical knowledge.
• Regulatory Approval: If the treatment proves to be safe and effective, it may be submitted for regulatory approval from health authorities before becoming available to the public.
• Ethical Considerations: Clinical trials adhere to strict ethical guidelines to protect the rights and well-being of participants. Institutional Review Boards (IRBs) or Ethics Committees review and approve the study protocols to ensure participants’ safety and privacy.

By following these steps, clinical trials provide critical evidence for deciding which treatments are safe and beneficial, advancing medical knowledge, and improving patient care. Tandem Clinical Research is proud to be part of this important process.

What Can a Study Participant Expect?

As a participant in a clinical trial, you can expect a structured and carefully monitored experience aimed at evaluating the safety and effectiveness of a new medical treatment, drug, or intervention. Here’s what you can typically expect:

• Informed Consent: Before joining the trial, you will be given detailed information about the study, including its purpose, procedures, potential risks, benefits, and your rights as a participant. This is known as the informed consent process. Take your time to review the information, ask questions, and ensure you understand everything before giving your consent.
• Screening Process: You’ll undergo a screening process to determine if you meet the specific eligibility criteria for the trial. These criteria may include age, gender, medical condition, medical history, and current health status.
• Randomization and Assignment: If you meet the criteria and agree to participate, you may be randomly assigned to one of the treatment groups. This randomization ensures unbiased and fair comparisons between different treatments.
• Study Procedures: Depending on the phase of the trial, you may receive the new treatment being tested, a standard treatment, or a placebo (if applicable). The trial’s procedures, including dosages, frequency of treatments, and follow-up visits, will be clearly explained to you.
• Monitoring and Follow-up: Throughout the trial, you will be closely monitored by healthcare professionals. They will conduct regular check-ups, tests, and assessments to track your progress and the treatment’s effects.
• Adherence to Protocol: It’s essential to follow the trial’s protocol and any instructions given by the research team. This consistency ensures the trial’s accuracy and reliability.
• Possible Risks and Side Effects: Be aware of potential risks and side effects associated with the treatment. The research team will inform you about these during the informed consent process and will be available to address any concerns you may have during the trial.
• Continued Medical Care: Even though you’re participating in a trial, you will continue to receive medical care for your condition. The research team will coordinate with your primary healthcare provider to ensure your well-being.
• Privacy and Confidentiality: Your privacy will be protected, and your personal information will be kept confidential in accordance with ethical guidelines and privacy laws.
• Open Communication: Feel free to communicate openly with the research team about any changes in your health, questions, or concerns. They are there to support and guide you throughout the trial.
• Voluntary Participation: Remember that participating in a clinical trial is entirely voluntary. You have the right to withdraw from the trial at any time without any penalty or impact on your regular medical care.

Clinical trials play a crucial role in advancing medical knowledge and improving patient care, and your participation contributes to these important efforts. Tandem Clinical Research takes great care to ensure your safety and well-being are the top priorities throughout the entire trial process.

Benefits of Participating In A Clinical Trial

Participating in a clinical research study offers several benefits, not just for the individual participant but also for the advancement of medical knowledge and the improvement of healthcare as a whole. Some of the key benefits include:

• Access to New Treatments: Participants in clinical research studies often get access to cutting-edge treatments, drugs, or interventions that may not be available through regular medical channels. This provides an opportunity to explore potential benefits not yet widely accessible.
• Advancing Medical Knowledge: By participating in research, individuals contribute directly to the expansion of medical knowledge. The data collected from the study helps researchers and healthcare professionals better understand diseases, their causes, and potential treatments.
• Improved Personal Healthcare: The careful monitoring and follow-up involved in clinical research can lead to a deeper understanding of the participant’s health condition. This can result in better disease management and personalized healthcare recommendations.
• Close Medical Supervision: Participants receive close medical supervision and attention from qualified healthcare professionals throughout the study. This frequent monitoring can identify health issues or concerns early on and allow for prompt intervention.
• Helping Others: Clinical research studies are essential for finding new and better treatments for various medical conditions. By participating, individuals directly contribute to the development of therapies that may benefit future patients and improve overall public health.
• Access to Expert Care: Clinical trials are often conducted at major medical centers and research institutions, where participants can receive care from expert healthcare providers and researchers.
• Cost Savings: In some cases, participating in a clinical trial may reduce the cost of treatment, as the study sponsor may cover some or all of the expenses related to the trial.
• Support and Education: Participants are provided with information and education about their condition and the treatment being studied. This empowers them to make informed decisions about their healthcare.
• Opportunity for Rare Conditions: For individuals with rare or challenging medical conditions, clinical trials may offer one of the few opportunities to explore potential treatments tailored to their specific needs.
• Contribution to Society: Being part of a clinical research study is a way of giving back to society and making a significant impact on the future of medicine and healthcare.

It’s important to note that while there are many benefits, clinical research also involves potential risks, and not every study may be suitable for every individual. Before deciding to participate in a clinical trial, it is crucial to carefully review the study information, ask questions, and discuss with the research team and your healthcare provider to make an informed choice.

Clinical trials are a crucial part of clinical research that test new medical treatments, drugs, or interventions on human participants to determine their safety and effectiveness. Here’s how they work: 1. Study Design: Before a clinical trial begins, researchers carefully plan and design the study. They define the objectives, eligibility criteria for participants, and the treatment plan. This design ensures that the trial produces reliable and meaningful results. 2. Phases of Clinical Trials: Clinical trials are typically conducted in multiple phases: a. Phase 1: These trials involve a small number of healthy volunteers to assess the treatment’s safety, dosage, and potential side effects. b. Phase 2: In this stage, the treatment is given to a larger group of patients who have the specific condition the treatment aims to address. Researchers monitor its effectiveness and further evaluate its safety. c. Phase 3: The treatment is tested on an even larger group of patients to compare its effectiveness against existing standard treatments or placebos. This phase provides more comprehensive data on safety and efficacy. d. Phase 4: After the treatment receives regulatory approval, Phase 4 trials are conducted to monitor its long-term safety and effectiveness in a broader population. 3. Randomization: Participants are randomly assigned to different groups. For example, in a Phase 3 trial, some participants might receive the new treatment while others receive the standard treatment or a placebo. This randomization helps minimize bias and ensures fair comparisons. 4. Blinding (Masking): Blinding means that participants and/or researchers may not know which treatment each participant is receiving. This prevents bias and helps obtain more objective results. Trials can be single-blind (participants don’t know), double-blind (neither participants nor researchers know), or open-label (both know). 5. Informed Consent: Before joining a clinical trial, participants must receive detailed information about the study, including potential risks and benefits. They give their informed consent to participate voluntarily. 6. Monitoring and Data Collection: Throughout the trial, researchers closely monitor participants’ health and collect data on their responses to the treatment. This includes regular check-ups, tests, and questionnaires. 7. Analysis and Results: After the trial is completed, researchers analyze the data to determine the treatment’s effectiveness and safety. The results are usually published in scientific journals, contributing to medical knowledge. 8. Regulatory Approval: If the treatment proves to be safe and effective, it may be submitted for regulatory approval from health authorities before becoming available to the public. 9. Ethical Considerations: Clinical trials adhere to strict ethical guidelines to protect the rights and well-being of participants. Institutional Review Boards (IRBs) or Ethics Committees review and approve the study protocols to ensure participants’ safety and privacy. By following these steps, clinical trials provide critical evidence for deciding which treatments are safe and beneficial, advancing medical knowledge, and improving patient care. Tandem Clinical Research is proud to be part of this important process.

As a participant in a clinical trial, you can expect a structured and carefully monitored experience aimed at evaluating the safety and effectiveness of a new medical treatment, drug, or intervention. Here’s what you can typically expect: 1. Informed Consent: Before joining the trial, you will be given detailed information about the study, including its purpose, procedures, potential risks, benefits, and your rights as a participant. This is known as the informed consent process. Take your time to review the information, ask questions, and ensure you understand everything before giving your consent. 2. Screening Process: You’ll undergo a screening process to determine if you meet the specific eligibility criteria for the trial. These criteria may include age, gender, medical condition, medical history, and current health status. 3. Randomization and Assignment: If you meet the criteria and agree to participate, you may be randomly assigned to one of the treatment groups. This randomization ensures unbiased and fair comparisons between different treatments. 4. Study Procedures: Depending on the phase of the trial, you may receive the new treatment being tested, a standard treatment, or a placebo (if applicable). The trial’s procedures, including dosages, frequency of treatments, and follow-up visits, will be clearly explained to you. 5. Monitoring and Follow-up: Throughout the trial, you will be closely monitored by healthcare professionals. They will conduct regular check-ups, tests, and assessments to track your progress and the treatment’s effects. 6. Adherence to Protocol: It’s essential to follow the trial’s protocol and any instructions given by the research team. This consistency ensures the trial’s accuracy and reliability. 7. Possible Risks and Side Effects: Be aware of potential risks and side effects associated with the treatment. The research team will inform you about these during the informed consent process and will be available to address any concerns you may have during the trial. 8. Continued Medical Care: Even though you’re participating in a trial, you will continue to receive medical care for your condition. The research team will coordinate with your primary healthcare provider to ensure your well-being. 9. Privacy and Confidentiality: Your privacy will be protected, and your personal information will be kept confidential in accordance with ethical guidelines and privacy laws. 10. Open Communication: Feel free to communicate openly with the research team about any changes in your health, questions, or concerns. They are there to support and guide you throughout the trial. 11. Voluntary Participation: Remember that participating in a clinical trial is entirely voluntary. You have the right to withdraw from the trial at any time without any penalty or impact on your regular medical care. Clinical trials play a crucial role in advancing medical knowledge and improving patient care, and your participation contributes to these important efforts. Tandem Clinical Research takes great care to ensure your safety and well-being are the top priorities throughout the entire trial process.

Participating in a clinical research study offers several benefits, not just for the individual participant but also for the advancement of medical knowledge and the improvement of healthcare as a whole. Some of the key benefits include: 1. Access to New Treatments: Participants in clinical research studies often get access to cutting-edge treatments, drugs, or interventions that may not be available through regular medical channels. This provides an opportunity to explore potential benefits not yet widely accessible. 2. Advancing Medical Knowledge: By participating in research, individuals contribute directly to the expansion of medical knowledge. The data collected from the study helps researchers and healthcare professionals better understand diseases, their causes, and potential treatments. 3. Improved Personal Healthcare: The careful monitoring and follow-up involved in clinical research can lead to a deeper understanding of the participant’s health condition. This can result in better disease management and personalized healthcare recommendations. 4. Close Medical Supervision: Participants receive close medical supervision and attention from qualified healthcare professionals throughout the study. This frequent monitoring can identify health issues or concerns early on and allow for prompt intervention. 5. Helping Others: Clinical research studies are essential for finding new and better treatments for various medical conditions. By participating, individuals directly contribute to the development of therapies that may benefit future patients and improve overall public health. 6. Access to Expert Care: Clinical trials are often conducted at major medical centers and research institutions, where participants can receive care from expert healthcare providers and researchers. 7. Cost Savings: In some cases, participating in a clinical trial may reduce the cost of treatment, as the study sponsor may cover some or all of the expenses related to the trial. 8. Support and Education: Participants are provided with information and education about their condition and the treatment being studied. This empowers them to make informed decisions about their healthcare. 9. Opportunity for Rare Conditions: For individuals with rare or challenging medical conditions, clinical trials may offer one of the few opportunities to explore potential treatments tailored to their specific needs. 10. Contribution to Society: Being part of a clinical research study is a way of giving back to society and making a significant impact on the future of medicine and healthcare. It’s important to note that while there are many benefits, clinical research also involves potential risks, and not every study may be suitable for every individual. Before deciding to participate in a clinical trial, it is crucial to carefully review the study information, ask questions, and discuss with the research team and your healthcare provider to make an informed choice.

Current Studies

Continuous Glucose Monitor Study – Marrero

Atopic Dermatitis Research Study – Metairie

Osteoarthritis Research Study – Metairie

Gastroparesis – Marrero

Alzheimer’s Disease – Metairie

Type 2 Diabetes Research Study

Why Tandem Clinical Research?

And the remedy starts with you! By participating in a clinical trial, you get the opportunity to access innovative treatments, advance medical knowledge, and contribute to improving healthcare for themselves and future generations.

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This content is for informational and educational purposes only. It is not intended to provide medical advice or to take the place of such advice or treatment from a personal physician. All readers/viewers of this content are advised to consult their doctors or qualified health professionals regarding specific health questions. Policylab.us does not take responsibility for possible health consequences of any person or persons reading or following the information in this educational content. All viewers of this content, especially those taking prescription or over-the-counter medications, should consult their physicians before beginning any nutrition, supplement or lifestyle program

Harbor-UCLA doctor is fired after county finds he regularly gawked at patients’ genitalia

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A premier L.A. County teaching hospital has fired one of its highest-ranking doctors following a two-year investigation that found he regularly gawked at the genitalia of anesthetized patients and never disclosed that he was being paid by a medical device company whose products he used on patients.

Staff members at Harbor-UCLA Medical Center, a public hospital run by the county, told investigators that Dr. Louis Kwong sometimes looked under the surgical covers of Black males who were under anesthesia and discussed the “genitals of the day,” according to his discharge notice, which was obtained by The Times.

Kwong also discussed his favorite sex positions and his preference for “auto-erotic asphyxiation,” his colleagues told investigators.

Additionally, investigators found that Kwong, an orthopedic surgeon, received more than $700,000 from the medical device company Zimmer Biomet, which makes joint replacements, without reporting the conflict of interest to the county. He flew twice on the company’s private plane to its Indiana headquarters with medical residents from the hospital, according to the Feb. 27 notice informing him of his firing.

The discharge notice makes no mention of the gun that Kwong, a volunteer deputy sheriff, had allegedly carried in the operating room and other parts of the hospital, according to a lawsuit filed by colleagues in October. The notice does say that he violated county policy by bringing a personal knife into the operating room on at least one occasion.

“Your inappropriate, disparaging comments and actions were offensive, and created an uncomfortable, hostile, and demoralizing work environment for others,” Griselda Gutierrez, the hospital’s chief medical officer, wrote in the notice.

Much of the misconduct described in the notice had been reported years ago to the county, raising questions about the inaction of hospital leaders. Kwong’s secretary complained more than a decade ago that her boss would remark on the grooming of anesthetized patients’ pubic hair, The Times previously reported . A doctor flagged Kwong’s conflict of interest with Zimmer Biomet to the health department’s chief medical officer in 2016, according to emails reviewed by The Times.

Yet the hospital didn’t launch an investigation until fall 2021, when it said accusations against Kwong were first “officially reported.” Kwong was placed on paid leave the following spring, as Sheppard Mullin, a law firm hired by the county, spent more than two years investigating him.

County policy requires departments in most cases to keep paying an employee who is on leave during an investigation. The slow pace allowed Kwong to receive more than a million dollars without working. In 2023 — a year in which Kwong didn’t work a single day — he was the eighth highest paid county employee, according to salary records posted this month.

Allegations of sexual harassment, armed surgeon roil top L.A. teaching hospital

The renowned teaching hospital Harbor-UCLA Medical Center is placed on probation amid lawsuits filed by prominent doctors alleging harassment and retaliation.

Nov. 3, 2023

Between 2021 and 2023, the county received seven more complaints about Kwong, according to his discharge notice. Harbor-UCLA, which treats largely poor and uninsured patients from around the South Bay, has been on probation since last summer after residents complained to an organization that oversees teaching hospitals of an “unprofessional and toxic work environment” in the orthopedics department, which Kwong chaired. The hospital is one of just six teaching hospitals across the nation that is on probation.

Kwong appealed his firing March 20 to the Civil Service Commission, a county body that can overturn disciplinary decisions. In a letter to the commission, Kwong’s attorney said her client denied or had no recollection of nearly all the allegations of inappropriate conduct and believed he was at risk of becoming the county’s “scapegoat.”

“Dr. Kwong disagrees with the County’s decision to terminate his employment and denies the manufactured allegations against him,” attorney Michelle Finkel Ferber wrote in an email to The Times. “Dr. Kwong looks forward to defeating these sensationalized claims through the appeals process, not in the press.”

Besides his consulting work for Zimmer Biomet, Kwong was dinged by the county for not disclosing his employment with the Lundquist Institute, a private research facility next door to Harbor UCLA. Many Harbor doctors also work as scientists at the institute.

“Zimmer Biomet and Lundquist not only compensated you for your work but provided you with financial incentives for business referrals, which created a clear conflict of interest since the Department had contracts with them,” the notice said. “Your decision to hide your employment with these companies for 6 years demonstrates your propensity for dishonesty.”

In a letter appealing Kwong’s discharge, Ferber said her client was never compensated by the Lundquist Institute, and there was no “intent to conceal the relationship with Zimmer Biomet.” The lack of disclosure was based on a misunderstanding of county policy, the attorney wrote.

The letter also stated that Kwong preferred Zimmer Biomet devices over other implants “based on their clinical record and performance outcomes.”

“Kwong’s decisions regarding implant choice are governed by what is best for addressing the patient’s reconstruction needs,” the letter said.

Some doctors say Kwong’s affiliation with both the Lundquist Institute and Zimmer Biomet was hardly a secret. Until recently, a Google search for “Dr. Louis Kwong” brought up his page on the Lundquist Institute’s site as one of the first results. Kwong was also listed as an “affiliate doctor” on Zimmer Biomet’s website, according to the discharge notice.

The Lundquist Institute has since taken down Kwong’s page. The Times could no longer find Kwong on Zimmer Biomet’s website.

According to the discharge notice, the county’s internal investigators began examining Kwong’s relationship with Zimmer Biomet after a complaint in 2021. But emails obtained by The Times show the issue was flagged for the county five years earlier.

On July 26, 2016, Tim Ryan, a former doctor with Harbor-UCLA who has since sued the county, emailed several colleagues screenshots from ProPublica’s Dollars for Docs portal, which shows payments disclosed by medical device companies to doctors.

Ryan sent entries for several county doctors, including Kwong, whose showed he had received payments from Zimmer Biomet.

Ryan’s email was forwarded to Hal Yee, chief medical officer for the Department of Health Services.

“Let’s discuss,” Yee responded. “I am concerned about both [conflict of interest] and failure to disclose.”

The Department of Health Services did not immediately respond to questions about the steps it took to follow up.

Two years later, Kwong posted a photo on his Facebook page of himself and his residents in front of a small plane, writing that he was on his way to Warsaw, Ind., where Zimmer Biomet is headquartered.

The same image was later posted on a bulletin board at Harbor, according to a photo of the board viewed by The Times.

After joining the county in 2007, Kwong ascended through the orthopedic department, nabbing the plum assignments of department chair and program director for residents. He received glowing performance reviews his last two years on the job, according to his discharge notice, with evaluators noting that he had “far exceeded expectations.”

But his rise was dogged by complaints that often went ignored.

In 2013, Maria Garibay, then a medical secretary, told the county’s human resources department that Kwong would have discussions with his staff about the women he operated on and “the variations in which they groom their pubic areas.” In 2019, a medical student accused Kwong of entering an operating room to peek “under the hood” and look at a patient’s genitalia. The comments, posted on a site used to rate orthopedic programs, were flagged for the hospital’s director of risk management, who responded that they had “started working on this.”

Some doctors say the 10-year delay in addressing complaints not only put the hospital in jeopardy but allowed a culture rife with racism and inappropriate behavior to fester.

According to Kwong’s discharge notice, three people told investigators that residents referred to Black patients as BAP, which reportedly stood for “Black Angry Patients.” Two doctors stated that Kwong compared two Black residency candidates as “brother versus brother.” During a meeting, a resident stated that a Black candidate “looked like he raped cheerleaders,” the notice stated. Another doctor used a racial slur in a text message.

The notice also paints a picture of a department with a locker-room atmosphere, where Kwong and some of his staff were fixated on the genitalia of patients.

Male genitalia were shown at an annual end-of-year “roast,” a doctor told investigators, where it “was commented that certain female residents like it on top.”

A technician once told the surgical team to “check out” an anesthetized patient’s penis because it was “very large,” leading Kwong to lift the surgical drapes, the notice said. A doctor heard Kwong discuss whether a patient was a “grower or shower,” and a physician assistant said Kwong joked about looking at genitalia of Black male patients while they slept.

Staff also told investigators that Kwong compared conducting a hip replacement to “finding the ‘G-spot,’ ” made a sexual innuendo about “hammering a patient” and commented on the fat rolls of female patients.

Some of these allegations about the orthopedics department burst into public view last year after three doctors sued the county, saying they were tired of watching complaints against Kwong stall.

Jennifer Hsu, one of the three doctors, said she had been told nothing about Kwong’s departure despite sitting for hours in interviews with investigators.

“They’ve been extremely opaque — it appears deliberately so,” she said.

The Department of Health Services declined to answer questions about Kwong — including whether he was given a severance payment or could receive a pension — and would confirm only that he no longer worked with the county. The department said in a statement that it could not comment on personnel matters but that Harbor-UCLA has “zero tolerance” for misconduct by staff.

“We have established clear channels for reporting allegations of misconduct so they can be thoroughly investigated,” the department said. “We wish to express our gratitude to those who utilized this process to bring their concerns to our attention.”

To Garibay, the statement rings hollow. In the aftermath of her 2013 complaint, she said, she was transferred to a different office, away from Kwong.

“They just brushed everything underneath the carpet,” she said. “I want everyone to know how dirty the county did me.”

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Rebecca Ellis covers Los Angeles County government for the Los Angeles Times. Previously, she covered Portland city government for Oregon Public Broadcasting. Before OPB, Ellis wrote for the Miami Herald, freelanced for the Providence Journal and reported as a Kroc fellow at NPR in Washington, D.C. She graduated from Brown University in 2018. She was named a finalist for the 2022 Livingston Awards for her investigation into abuses within Portland’s private security industry.

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Breaking news, onlyfans creator farha khalidi claims she was paid to spread ‘political propaganda’ for biden admin.

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An OnlyFans creator and TikTok star has claimed she was paid to spread “political propaganda” for the Biden administration on social media — and that she was asked to hide the fact it was advertising.

Farha Khalidi said she’d been asked to help boast about then-Judge Ketanji Brown Jackson to her tens of thousands of social media followers after Brown Jackson was nominated to the Supreme Court by President Biden.

“I was doing full-on political propaganda,” the social media personality said during a recent podcast interview with commentator  Richard Hanania .

Farha Khalidi on how surrogates for the Biden administration tried to pay her to engage in identity politics and sell their message. A case of racial division as a top-down phenomenon. They're literally buying the TikTok influencers. pic.twitter.com/nJWGvsLlMu — Richard Hanania (@RichardHanania) April 26, 2024

“The funny thing is they’re, like, ‘Do not disclose this as an ad’ because they [were], like, ‘Technically, it’s not a product, so you don’t have to disclose it’s an ad.’ Because I think they just wanted, like, some edgy girl of color to just tell people — like when they nominated Ketanji Brown Jackson, they’re, like, ‘Can you say “as a person of color,” you know, that you feel “reflected”?’”

When probed about the Biden admin, Khalidi, who boasts more than 119,000 Instagram followers, clarified that she was dealing with a “conduit” third-party media company at the time.

“It’s not Biden, but it’s, like, a third party. You know what I mean? It’s, like, a media company that’s doing it on his behalf. I’m not blaming him for this,” Khalidi said.

She went on to say that she ultimately pushed back against the “script” because it was a white woman from the media company telling her what to say.

“And I’m, like, ‘No,’ and she’s like, ‘Please,’ and I’m like, ‘No.’ I’ll talk about the news of it, but I’m not gonna be like — I’m not gonna have a white person tell me to be, like, ‘This is how I feel as a person of color.’ It’s just so — I think that black-pilled me slightly on political propaganda,” Khalidi said.

“Yeah, they’re basically, ‘As, like, another black person, can you just say that you feel reflected by Ketanji?’ I’m like, ‘No, I’ll talk about Ketanji’s background and her accomplishments,’ but you know what I mean? I’ll never — I’m not gonna say, like, the corny stuff, even if it was a brown person emailing it to me.”

The White House didn’t immediately respond to The Post’s request for comment.

Elsewhere in the interview, Khalidi said the political payments were just one way she was raking in cash during college.

“I was taking ads by the time I graduated college from, like, the Biden administration, Planned Parenthood and, like, dating apps and stuff. So it was, like, fully financially sustaining me,” Khalidi said.

It wasn’t immediately clear exactly how much Khalidi was paid.

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Anthony Davis' Current Injury Status For Lakers-Nuggets Game

Anthony Davis is on the injury report for Game 5.

• Author: Ben Stinar

UPDATE: Anthony Davis is available.

On Monday evening, the Los Angeles Lakers will be in Denver to face off against the Nuggets for Game 5 of their first-round playoff series.

For the game, the Lakers have listed Anthony Davis as probable, so he should be available.

Via Rotoworld Basketball: "LeBron James, Anthony Davis probable for Monday"

LeBron James, Anthony Davis probable for Monday https://t.co/pMqsVradEX — Rotoworld Basketball (@rotoworld_bk) April 21, 2024

Davis is coming off another fantastic regular season where he averaged 24.7 points, 12.6 rebounds, 3.5 assists, 1.2 steals and 2.3 blocks per contest while shooting 55.6% from the field and 27.1% from the three-point range in 76 games.

The Lakers are the seventh seed in the Western Conference and had a 47-35 record (they beat the New Orleans Pelicans in the play-in tournament).

They are coming off a season where they were swept by the Nuggets in the Western Conference Finals.

Apr 27, 2024; Los Angeles, California, USA; Los Angeles Lakers forward Anthony Davis (3) shoots

Jason Parkhurst-USA TODAY Sports

Currently, the Lakers are down 3-1 to the Nuggets after winning Game 4 by a score of 119-108 (at home).

Davis finished with 25 points, 23 rebounds, six assists and one block while shooting 11/17 from the field in 42 minutes of playing time.

Now Watching: Top Plays from Game 4 🎬 @MichelobULTRA x #LakeShow pic.twitter.com/XRD4XWkR2u — Los Angeles Lakers (@Lakers) April 29, 2024

Game 6 of the series would be on Thursday evening in Los Angeles.

Whoever wins the series will advance to the second round and face off against Anthony Edwards and the Minnesota Timberwolves (who swept the Phoenix Suns).

Monday work pic.twitter.com/pdo2jc86ac — Los Angeles Lakers (@Lakers) April 29, 2024

As for the Nuggets, they are the second seed in the Western Conference and had a 57-25 record.

They are coming off a year where they defeated Jimmy Butler and the Miami Heat to win the 2023 NBA Championship.

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