Register Study

ClinicalTrials.gov is a registry and results database of publicly and privately supported clinical studies of human participants conducted around the world. As required by federal law, all IRB approved drug and biologic studies must be registered, with the exception of those which are Phase 1 studies.

Also, all IRB approved medical device trials must be registered, with the exception of small feasibility studies and pediatric post marketing surveillance studies. After registering the trial, it is the responsibility of the researcher to keep all study specific information on the website up to date.

The ClinicalTrials.gov website is very informative, clarifies which studies must be registered and gives step by step instructions on how to do so. Please follow the link below to Clinicaltrials.gov and click on the "Submit Studies" tab, followed by "How to Register Your Study" to start the process.

For further assistance with registering a clinical trial, please submit a consultation request for support from a member of the Office of Research & Innovation before visiting the ClinicalTrials.gov website.