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Service Description

The Trial Registration Service provides a standardized set of interfaces for registering Trials with NCI's Clinical Trials Reporting Program (CTRP). There are two main categories of clinical trials that can be registered with CTRP - NCI-supported trials (also referred to as Complete trials) and Industry-led (referred to as 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

Obtain 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 service specifications can be downloaded from this location: Service Specifications
  • 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.
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