All Current Studies

Study

Gender

Age

Compensation

Acne Ongoing

M / F

 

TBD

Alcohol Use Disorder Ongoing

M / F

 

TBD

Allergies Ongoing

M / F

 

TBD

Alzheimer’s Disease Ongoing

M / F

 

TBD

Atopic Dermatitis Ongoing

M / F

 

TBD

Attention Deficit Hyperactivity Disorder (ADHD) Ongoing

M / F

 

TBD

Binge Eating Disorder Ongoing

M / F

 

TBD

Bipolar Ongoing

M / F

 

TBD

Borderline Personality Disorder Ongoing

M / F

 

TBD

Chinese Bridging Studies Ongoing

M / F

 

TBD

Chronic Kidney Disease Ongoing

M / F

 

TBD

Chronic Pain Ongoing

M / F

 

TBD

Cocaine Use Disorder Ongoing

M / F

 

TBD

Cognitive Impairment Ongoing

M / F

 

TBD

COPD Ongoing

M / F

 

TBD

Covid-19 Vaccine Trials Ongoing

M / F

 

TBD

Crohn’s Disease Ongoing

M / F

 

TBD

Depression Ongoing

M / F

 

TBD

Diabetes Ongoing

M / F

 

TBD

Dyslipidemia Ongoing

M / F

 

TBD

Excessive Daytime Sleepiness Ongoing

M / F

 

TBD

Fibromyalgia Ongoing

M / F

 

TBD

Generalized Anxiety Disorder (GAD) Ongoing

M / F

 

TBD

Healthy Adult Studies Ongoing

M / F

 

TBD

Hot Flashes Ongoing

M / F

 

TBD

Hypercholesterolemia Ongoing

M / F

 

TBD

Hypersomnia Ongoing

M / F

 

TBD

Hypertension Ongoing

M / F

 

TBD

Insomnia Ongoing

M / F

 

TBD

Irritable Bowel Syndrome (IBS) Ongoing

M / F

 

TBD

Japanese Bridging Studies Ongoing

M / F

 

TBD

Methamphetamine Use Disorder Ongoing

M / F

 

TBD

Migraine Ongoing

M / F

 

TBD

Molluscum Contagiosum Ongoing

M / F

 

TBD

Multiple Sclerosis Ongoing

M / F

 

TBD

Narcolepsy Ongoing

M / F

 

TBD

Neuropathic Pain Ongoing

M / F

 

TBD

Nonalcoholic Fatty Liver Disease (NAFLD) Ongoing

M / F

 

TBD

Nonalcoholic Steatohepatitis (NASH) Ongoing

M / F

 

TBD

Obesity Ongoing

M / F

 

TBD

Obsessive Compulsive Disorder (OCD) Ongoing

M / F

 

TBD

Opioid Use Disorder Ongoing

M / F

 

TBD

Osteoarthritis Ongoing

M / F

 

TBD

Parkinson’s Disease Ongoing

M / F

 

TBD

Post Traumatic Stress Disorder (PTSD) Ongoing

M / F

 

TBD

Post-Menopausal Females Ongoing

M / F

 

TBD

Post-Stroke Ongoing

M / F

 

TBD

Postpartum Depression Ongoing

M / F

 

TBD

Pruritus Ongoing

M / F

 

TBD

Psoriasis Ongoing

M / F

 

TBD

Restless Leg Syndrome Ongoing

M / F

 

TBD

Rosacea Ongoing

M / F

 

TBD

Schizophrenia/Schizoaffective Ongoing

M / F

 

TBD

Sleep Apnea Ongoing

M / F

 

TBD

Smoking Cessation Ongoing

M / F

 

TBD

Social Anxiety Disorder (SAD) Ongoing

M / F

 

TBD

Spinocerebral Ataxia (SCA) Ongoing

M / F

 

TBD

Tobacco Users Ongoing

M / F

 

TBD

Tourette’s Syndrome Ongoing

M / F

 

TBD

Treatment-resistant Depression Ongoing

M / F

 

TBD

Volunteer for a Clinical Trial

If you are interested in one of our studies or would like to inquire about upcoming clinical trials, please call Patient Recruitment for more information between 7am - 5pm Monday - Friday.

Call 866-787-4257 now or fill in the form below and we will contact you:

Qualified participants will receive free medical care related to the study and may receive financial compensation for time and travel expenses. Enrollment is limited.
Please call 866-787-4257 for details or fill out the form above.

State-of-the-Art Facilities

CenExel CNS is one of our premier clinical research facilities in California. For over a decade, we’ve helped improve the quality of life for everyone by researching new medications and treatments. Our state-of-the-art facility is held to the highest standards of cleanliness and quality.

Board-Certified Physicians

Your safety is our greatest concern. Every procedure at CenExel CNS is overseen by expert medical staff and performed by some of the most well-respected board-certified physicians in the industry, each with many years of experience in their respective specialties.

FDA-Approved Procedures

Rest assured, you are not signing up for treatment with “experimental” methods. iResearch only uses FDA-approved methods as if you were at any other hospital or clinic. Our research is focused on the medication associated with those methods.

Frequently asked questions

What is a CenExel Center of Excellence?

CenExel Centers of Excellence provide unparalleled medical and scientific support in the design and execution of clinical trials. Their attention to detail assures quality, reliable results and has helped CenExel to consistently achieve and exceed patient recruitment goals. They have conducted thousands of studies, the variety and complexity of which have resulted in a great depth of experience and insight for the principal investigators and research staff in each facility. CenExel Centers of Excellence deliver the engagement, expertise, and results to ensure that clients achieve their clinical research goals.

How do clinical trials work?

The study procedures and process will vary depending on the type of clinical trial you participate in. Before you begin a study, the process and all procedures for that study will be explained to you. Throughout the study, the Study Coordinator and the Principal Investigator will assist you and can answer any questions you have. They will check your health at the beginning of the trial, give you specific instructions for participating in the trial, monitor you carefully during the trial, and stay in touch with you after the study.

Some clinical trials involve more tests and doctor visits than you would normally have for your illness or condition. Your participation will be most successful if you carefully follow all instructions you are given and stay in contact with the research staff.

How safe are clinical studies?

There are many safeguards in place that all companies must follow when conducting clinical trials.

The Food and Drug Administration (FDA) is the regulatory agency that oversees all clinical research conducted in the United States. It is their responsible to protect the rights and as much as possible, the welfare of subjects participating in clinical trials. They ensure that data collected from clinical trials is of the highest quality and they are the agency that determines whether a new treatment should be sold in the US. Several organizations and individuals are governed by FDA regulations including clinical investigators, sponsors (the companies developing the treatments), Contract Research Organizations (companies that help conduct the studies), and Institutional Review Boards (groups that are responsible for ensuring the safety and welfare of study participants).

Good Clinical Practice (GCP) guidelines are another safeguard implemented to protect the safety of subjects. These guidelines encompass federal regulations and industry-accepted standards that govern clinical trials on humans. These regulations and standards apply to the conduct of the studies, record keeping, informed consent of subjects, collection of scientific data, and submission of information needed for the FDA to determine whether a new treatment should or should not be sold in the US. All companies must follow these guidelines when conducting clinical research.

An Institutional Review Board (IRB) is a committee that is formally tasked by an institution to review, approve, and monitor research involving human subjects. IRBs ensure that the risks to subjects are minimized; that subjects are adequately informed about the trial and the implications it will have on their treatment; that study protocols are modified, when necessary, to ensure safety; that risks are reasonable in relation to the anticipated benefits and the importance of the knowledge to be gained; that subject selection is equitable and that no classes of patients are discriminated against; that informed consent is obtained; that there is a provision for safety monitoring in the research plan; and that here are adequate provisions for the privacy and confidentiality for subjects and the data collected.

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