Clinical research studies (often also called trials or protocols) are a method of developing new treatments and/or medications for diseases and conditions.

The health of millions of people has improved thanks to scientific and technological advances, and the willingness of thousands of people like you to participate in clinical research. The role of volunteers as collaborators in clinical research is crucial in the pursuit of knowledge that will improve the health of future generations. Without their help, research studies at the Clinical Center could not be conducted. (Provided by the NIH, National Institutes of Health)

No, health insurance is not required to participate in any clinical trial. If you are accepted into the study, our board-certified and eligible physicians and staff will provide you with the necessary medications and medical care.

No, there is no cost to participate. Participants who meet all study criteria may receive compensation for their time and travel expenses related to their participation. This compensation varies depending on the study in which they participate.

Some studies compare the drug being tested in one group with another group taking a placebo (a similar pill or tablet without any active ingredient). You will be informed if the study you are considering includes a placebo so you can make an informed decision about whether or not to participate.

A board-certified or board-eligible physician and/or highly trained clinical research staff, working together, will provide you with medical supervision throughout your participation in the study.

The Food and Drug Administration (FDA) has strict guidelines and regulations that help ensure the safety of clinical trials. The FDA is a U.S. government agency charged with, among other things, overseeing the development of investigational drugs and medical devices. According to the FDA, "Carefully conducted clinical trials are the safest and fastest way to find effective treatments for people and new ways to improve health."

The commitment to a clinical trial ranges from a few weeks to several years. During your first visit, you'll be informed exactly what will be expected of you during the trial, so you can decide whether you want to continue with the screening process.

You can participate in one clinical study at a time. A 30-day waiting period is typically required before enrolling in another clinical trial.

We're constantly adding new studies. Contact us if you don't see the indication you're interested in, and we can check our portfolio of upcoming studies or add you to our database so we can contact you when we have something that fits your needs.

We maintain a HIPAA-compliant database used exclusively by CRWF to identify potentially eligible patients for current and future clinical trials. If you do not qualify for a current study, we will confirm your desire to be included in our database and contact you when an option becomes available.

Click here to see the studies currently offered