About the CTRP Wiki
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.
This wiki includes the following.
- 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
- Service Specifications - provides detailed information about CTRP services for developers
- Information for CTRP Application Users
- CTRP User Meetings - information, including meeting schedules and notes
- COPPA Core Services - information about, and instructions for accessing and using CTRP core services
- Information About the CTRP Project
- Application Release Plans and Schedules - information, including release notes for past and current releases; plans for future releases; and recurring meeting schedules
- CTRP Environments and Tiers - outlines the policies and procedures the CTRP team follows internally when deploying software to various tiers
- CTRP Project Team - lists project team members and their roles
- Overview of CTRP Applications - introductory information about applications, including those available for use by individuals registered in CTRP, and those for use by internal NCI/CTRP application specialists
- Information for CTRP Application Developers - information for developers and consumers of COPPA core services
- CTRP Dev Team Meeting Notes
- Technical Notes - provides design and development information for developers and architects
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.
For further information about CTRP, visit the NCI's CTRP Website.
Documentation and FAQs
- 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
- CTRP domain models
- Requirements and design documents
- Requirements documents
- NCI Commons software libraries - documentation about the NCI Commons software libraries used by the CTRP applications
- Requirements documents
- Project management documents - project management plan, communications plan, risk management plan, and project schedule
Lists and Forums
List/Forum |
Email address or URL |
Description |
|---|---|---|
https://cabig-kc.nci.nih.gov/CTMS/forums/viewforum.php?f=31&sid=91e58e81f9fd9124a6e43fca41dc7b39 |
General discussions about CTRP in the caBIG Knowledge Center |
|
https://cabig-kc.nci.nih.gov/CTMS/forums/viewforum.php?f=33&sid=91e58e81f9fd9124a6e43fca41dc7b39 |
Discussions about CTRP services in the caBIG Knowledge Center |
|
Discussions related to the design and development of CTRP applications and services. Limited to the CTRP development team |
||
CTRP USERS LIST (CTRP-Users-L@list.nih.gov) subscription requests |
General discussions about CTRP applications and services for CTRP users |
