NIH | National Cancer Institute | NCI Wiki  

WIKI MAINTENANCE NOTICE

Please be advised that NCI Wiki will be will be undergoing maintenance on Monday, June 24th between 1000 ET and 1100 ET.
Wiki will remain available, but users may experience screen refreshes or HTTP 502 errors during the maintenance period. If you encounter these errors, wait 1-2 minutes, then refresh your page.

If you have any questions or concerns, please contact the CBIIT Atlassian Management Team.

Versions Compared

Key

  • This line was added.
  • This line was removed.
  • Formatting was changed.
Comment: Attempting to update links to XSD files.

...

Section
Column
width40%
Panel
titleTopic Links

Table of Contents
maxLevel4
minLevel2

Column

This section provides instructions for registering, updating, and amending Complete and Abbreviated trials via the NCI CTRP Trial Registration REST Service.

Introduction

Trial Registration REST Service is a CTRP Web Service that provides the following operations in a REST-like fashion:

  • Register an Abbreviated trial in CTRP from ClinicalTrials.gov using a ClinicalTrials.gov Trial Identifier
  • Update an Abbreviated trial in CTRP
  • Register a Complete interventional or non-interventional trial in CTRP
  • Update a Complete trial in CTRP
  • Amend a Complete trial in CTRP

The service uses XML for data exchange.

Note
titleProgram Codes

The program codes feature (not to be confused with NCI Divisions Division and ProgramsProgram Values) has been enhanced. The system ignores program codes unless the trial is one of the following:

  • Complete trial with a lead organization as a member of your cancer center family of organizations.
  • Abbreviated trial where such a member is a participant.

The system validates program code values against those listed on the Manage Program Codes Master List page for your affiliated cancer center. For details, refer to Managing Program Codes.

...

The service uses XML for data exchange.All XML elements going in or out of the service are defined and validated against the following XML schemas:

XML schemas are well-annotated with inline documentation that explains the purpose and meaning of various elements, types, and attributes. These schemas specify which elements are required and the required order of those elements. Specific elements required for service operations are explained in the sections below.

...

Registering or amending Complete trials in the CTRP involves organizations and persons that have the following roles in clinical trials: lead organization, sponsor, principal investigator, and so on. CTRP does not manage information about persons and organizations; instead, this is delegated to the Person and Organization Curation Portal, also known as PO. For more information, refer to the Person and Organization Curation Portal User's Guide.

Note
You must have a user account with appropriate LDAP membership to access the PO User's Guide.

...