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The Trial Registration Service provides a standardized set of interfaces for registering Trials with NCI's Clinical Trials Reporting Program (CTRP). Please visit http://www.cancer.gov/ncictrp to learn more about NCI's CTRP. There are two main categories of clinical trials that can be registered with CTRP - NCI-supported trials (also referred to as non-proprietary Complete trials) and Industry-led or Investigator-initiated (referred to as Proprietary Abbreviated Trials). Please visit http://www.cancer.gov/ncictrp to learn more about NCI's CTRP.

The Trial registration service's semantic representation leverages the computable structured representation of a Study Protocol as defined by the BRIDG model and implemented in COPPA services as a BRIDG based Information model in support of computable semantic interoperability.

Prerequisites

1. Obtain a grid credential (Dorian User Account) by following the instructions on the web at: http://cagrid.org/display/cagrid13tutorials/Create+User+Account for instructions.
You can either create a new personal grid account, or log in as the existing "coppagridtest" account on the Training or Stage grids.

  • Developers working outside the NIH firewall must use the grid trust fabric, Training Grid.
  • Developers working inside the NIH firewall can use either the Training or Stage Grids.

2. Do self registration with the CTRP registration application https://trials-<<tier>>.nci.nih.gov/registry and use the email address in StudyProtocol.lastUserCreated valid user account for CTRP for the environment (Integration, Demo, Stage, or Production) that you intend to use.

Reference Documents

Refer to the following documents before consuming the service