This site contains information that will help you understand NCI's Clinical Trials Reporting Program (CTRP).

Learn more about NCI's CTRP initiative

Overview of the 2011-2012 CTRP reporting guidelines

Provides the main steps for registering trials, and links to Excel workbooks that help you to prepare your trial records for submission to the CTRP.

Answers questions relating to the purpose of CTRP and specific registration details

Contains CTRP User's Guides, a glossary of CTRP terms and acronyms; and other useful templates and documentation

Ready to register your trials?

When you are ready to register your trials, go to the
Clinical Trials Registration Site