Safety
Patient safety is a priority in every clinical study. Each trial follows strict safety rules and is reviewed by independent boards before the trial begins and throughout the trial process.
How are Participants Protected?
Independent safety experts, known as an Institutional Review Board (IRB), review and monitor trials to ensure risks are minimized and participants are protected. They can stop a study at any time if they believe it’s unsafe.
What About Side Effects?
All drugs and medical procedures carry a risk of side effects. The trial staff will explain these potential risks before you decide whether to participate, and will help address any concerns. Doctors will monitor your health throughout the trial, and will talk with you if there is any change in your medical condition while you are in the trial.
Can I Leave a Trial?
Participating in a clinical trial is always voluntary! You can stop being in a trial at any time and for any reason.
How the Process Works
Some information on this page has been adapted from the Center for Information and Study on Clinical Research Participation.