CenExel CNS is seeking volunteers living with cannabis addiction to participate in our clinical trial. Cannabis use disorder, or cannabis addiction, is the continued use of cannabis despite significant negative impact on one’s life and health. Individuals with...
CenExel CNS is seeking healthy volunteers to participate in our flu/COVID-19 vaccine clinical trial. This vaccine is being evaluated to help determine its effects against viruses. Coronavirus disease (COVID-19) is an infectious disease caused by the SARS-CoV-2 virus....
CenExel CNS is seeking volunteers living with panic disorder to participate in our clinical trial. Individuals with panic disorder experience spontaneous seemingly out-of-the-blue panic attacks and are very preoccupied with the fear of a recurring attack. Panic...
Healthy clinical research studies are exactly what the name implies, clinical research studies for healthy people. These clinical trials are generally early phase and are used to investigate how drugs or other forms of treatment are absorbed into the body. Are you...
Alzheimer’s disease and other forms of Dementia are not a normal part of aging, it is a disease and it is deadly. The early symptoms of Alzheimer’s are very similar to common symptoms of aging. You may notice that your memory and cognitive ability aren’t as good as...
Depression is characterized by feelings of hopelessness, a lack of energy, and decreased pleasure in normally enjoyable. Additional forms of depression include Major Depressive Disorder, Postpartum depression, treatment-resistant depression and it shares some symptoms...
Japanese Clinical Trials 臨床試験・治験ってなに？ 臨床試験とは、疾患の診断・治療・予防などの方法を改善するために「人」を対象にして行う研究のことをいいます。臨床試験の中でも新薬や新しい医療機器の製造承認を得るために行う試験のことを「治験」といいます。 医薬品・医療器具は、病院・医院で医師が処方箋を書いて使うことができるものを指しますが、これらについてFDA(US Food and Drug Administration)が製造を認可するに値するものであることを示すデータを提出することが治験の目的です。...
Parkinson’s Disease (PD) belongs to a group of conditions called motor system disorders, which are the result of the loss of dopamine-producing brain cells. PD impedes movement and often induces physical tremors in people who are affected, impeding daily life and...
Diabetes is characterized by hyperglycemia and glucose intolerance. Symptoms: Being very thirsty Urinating often Feeling very hungry or tired Losing weight without trying Having sores that heal slowly Having blurry eyesight
The pain of a migraine headache is often described as an intense pulsing or throbbing pain in one area of the head and is often accompanied by additional symptoms, such as nausea/vomiting or sensitivity to both light and sound. Symptoms: – Moderate to severe...
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.
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.
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.
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.