The Clinical Register

Standards

Clinical Research Registration Standards

Clinical Register adheres to international standards for clinical research registration, ensuring transparency and accountability.

WHO International Clinical Trials Registry Platform (ICTRP)

Our platform is designed to comply with the WHO ICTRP standards, which define the minimum registration dataset required for clinical trials:

  • Primary registry and trial identifying number
  • Date of registration in primary registry
  • Secondary identifying numbers
  • Source(s) of monetary or material support
  • Primary sponsor
  • Secondary sponsor(s)
  • Contact for public queries
  • Contact for scientific queries
  • Public title
  • Scientific title
  • Countries of recruitment
  • Health condition(s) or problem(s) studied
  • Intervention(s)
  • Key inclusion and exclusion criteria
  • Study type
  • Date of first enrollment
  • Target sample size
  • Recruitment status
  • Primary outcome(s)
  • Key secondary outcomes

CONSORT Statement

We encourage researchers to follow the CONSORT (Consolidated Standards of Reporting Trials) guidelines when preparing study protocols and reporting results.

Good Clinical Practice (GCP)

All registered studies should adhere to ICH-GCP guidelines, ensuring:

  • Protection of participant rights, safety, and well-being
  • Credibility of clinical trial data
  • Proper informed consent procedures
  • Independent ethics committee review

Data Transparency

We support the AllTrials campaign and advocate for:

  • Prospective registration of all clinical trials
  • Publication of full methods and results
  • Open access to clinical trial data