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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

Self-register to CTRP by going to https://trials-<<tier>>.nci.nih.gov/registry, replacing "<<tier>>" with the appropriate deployment tier you are working with: int for the integration tier, demo for the demo tier, stage for the stage tier, or leave out -<<tier>> completely for the production tierObtain a 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

• Trial Registration documents (CFSS, PIM , PSM), service specifications can be downloaded from this location: Service Specifications CTRP Web Services Guides v4.4
• Implementation materials for the Trial Registration service are available here: Trial Registration Sample Client
• A list of CTRP/COPPA roots to be used with ISO 21090 II can be found here.