ClinicalTrials.gov
ClinicalTrials.gov is a publicly accessible international database that registers clinical studies conducted worldwide. The system enables researchers to register their clinical studies, update study information, and submit study results.
Many international scientific journals and research funding organizations require clinical studies to be registered in ClinicalTrials.gov as a prerequisite for publication or funding.
Researchers affiliated with Istanbul Medipol University who wish to register their clinical studies in ClinicalTrials.gov must first create an individual PRS (Protocol Registration and Results System) account.
Individual PRS Account Application: https://register.clinicaltrials.gov/prs/app/template/ApplyIndAccount.vm
PRS Roles and Responsibilities: https://register.clinicaltrials.gov/prs/html/prs-users-guide.html#overviewrolesandresponsibilities
The following resources provide training materials and guidance for using ClinicalTrials.gov and the Protocol Registration and Results System (PRS):
- PRS Guided Tutorials: Step-by-step tutorials for registering clinical studies and submitting study results in the ClinicalTrials.gov PRS.
https://prsinfo.clinicaltrials.gov/tutorial/content/index.html#/ - ClinicalTrials.gov PRS Login (Investigator Login): https://register.clinicaltrials.gov
- PRS Help Resources: https://clinicaltrials.gov/submit-studies/prs-help
- ClinicalTrials.gov Protocol Review Criteria (PDF): Detailed review criteria used to evaluate clinical study registration records.
https://prsinfo.clinicaltrials.gov/ProtocolDetailedReviewItems.pdf - PRS User’s Guide: A comprehensive guide to using the PRS, including study registration and results submission.
https://clinicaltrials.gov/submit-studies/prs-help/user-guide
Son Güncelleme 14 August 2026
