NIHSeniorHealth: Participating in Clinical Trials

What is a Clinical Trial? Finding a Clinical Trial Informed Consent Should I Join a Clinical Trial? Frequently Asked Questions MedlinePlus for More Information Printer friendly version		Participating in Clinical Trials Frequently Asked Questions 26. What is informed consent? Click to enlarge image Informed consent is an ongoing process that helps you decide whether to enroll in a trial after you have been told all about the study. The informed consent document is an agreement to take part in a trial. (Answer continues on next page.)

		Return to list of Questions Next Page
Last reviewed: 03 January 2008 First published: 03 January 2008 National Institute on Aging, U.S. National Library of Medicine National Institutes of Health, U.S. Department of Health & Human Services Contact us, Accessibility, Copyright, Privacy