Clinical Trials Reporting Program
This site contains information that will help you understand NCI's Clinical Trials Reporting Program (CTRP).
Outlines the background and objectives of NCI's Clinical Trials Reporting Program (CTRP)
Provides information about trial registration with links to spreadsheets, templates, and other relevant information that will help you to prepare trial records for submission to CTRP
Answers many common questions about CTRP
Contains the CTRP User's Guides, a glossary of CTRP terms and acronyms, as well as specifications, templates, and other helpful documentation
When you are ready to register your trials, go to the
Clinical Trials Registration Site