Service Description
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 trials) and Industry-led or Investigator-initiated (referred to as Proprietary Trials). 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. Self-register to CTRP by going to https://trials-<<tier>>.nci.nih.gov/registry
Reference Documents
Refer the following documents before consuming the service
- Trial Registration (CFSS, PIM , PSM), can be downloaded from this location: Service Specifications
- Implementation materials for the Trial Registration service are available here: Trial Registration Sample Client