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:
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
Contact Lynn Jagodzinski, UB CTSI Clinical Research Regulatory Administrator, at email@example.com, or UB CTSI Quality Assurance Specialist Urmo Jaanimägi at firstname.lastname@example.org.
University at Buffalo’s ClinicalTrials.gov Registration and Results Guide: download
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
Contact any of the nine CTSI cores for a list of services and resources offered, and for answers to your research questions.