![]() |
Page History
...
This is the wiki home page for the Clinical Trials Reporting Program (CTRP). The purpose of this site is to provide up-to-date information on the development of the applications, tools, and services supporting the CTRP program. You are welcome to leave comments.
Excerpt
hidden | true |
---|
- Information for CTRP Application Users
- CTRP User Meetings - information, including meeting schedules and notes.
- CTRP FAQs - frequently asked questions, including how to submit feature requests and bugs.
- CTRP User's Guides - instructions for using each of the CTRP applications.
- COPPA Core Services - information about, and instructions for accessing and using CTRP core services.
- Information About the CTRP Project
- Information for CTRP Application Developers
About CTRP
NCI's Clinical Trials Reporting Program (CTRP) fulfills a recommendation made by the NCI Clinical Trials Working Group (CTWG) to the National Cancer Advisory Board. The purpose of the program is to establish a comprehensive database containing regularly updated information on all NCI-funded clinical trials. Grantees enter specific information about each clinical trial into the database. NCI internally transfers to CTRP information on CTEP, CCR and DCP trials, eliminating the need for awardees to enter information on these trials. NCI uses this information to coordinate research efforts to optimize our nation's investment in cancer research. NCI initiated a phased launch of CTRP, which started January 2009, with a focus on registering interventional trials only. The registration of observational, ancillary and correlative studies will begin at a later date.
Tip |
---|
For further information about CTRP, please visit the NCI's CTRP Website. |
Documentation and FAQs
Information for CTRP Application Users
Current Release
CTRP Version 3.7 is the current release; it is currently on Production.
...