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: 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.
