ClinicalTrials.gov: How to Register Your Trial

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Registering your study with ClinicalTrials.gov is a necessary step for investigators to be compliant with regulations. This UB CTSI Educational Modules video provides useful insights to the Protocol Registration and Results System (PRS) — making study registration less complicated — and also explores:

  • How do I get started with registering my study?
  • What happens if I do not register my clinical trial?
  • Useful resources

Developed by Lynn Jagodzinski, CTSI Clinical Research Regulatory Administrator, and Urmo “Mo” Jaanimägi, CTSI Quality Assurance Specialist

Presenter: Urmo “Mo” Jaanimägi, CTSI Quality Assurance Specialist, Clinical and Translational Science Institute
Running Time: 
30 minutes

Questions?

Contact Lynn Jagodzinski, UB CTSI Clinical Research Regulatory Administrator, at lynnjago@buffalo.edu, or UB CTSI Quality Assurance Specialist Urmo Jaanimägi at uj@buffalo.edu.

Additional resources:

University at Buffalo’s ClinicalTrials.gov Registration and Results Guide: http://www.buffalo.edu/content/dam/www/ctsi/Cores/RecruitmentSpecialPop/toolkit/ClinicalTrialsgov%20Registration%20and%20Results%20Guide%209.24.2021.pdf
How to Register Your Study — ClinicalTrials.gov: https://clinicaltrials.gov/ct2/manage-recs/how-register
PRS Guided Tutorials: https://prsinfo.clinicaltrials.gov/tutorial/content/index.html
Protocol Registration Data Element Definitions for Interventional and Observational Studies ­— ClinicalTrials.gov: https://prsinfo.clinicaltrials.gov/definitions.html
PRS User's Guide — ClinicalTrials.gov: https://prsinfo.clinicaltrials.gov/prs-users-guide.html