Short Course requires Pre-Registration and is an additional fee.
This short course covers the basics of using the ClinicalTrials.gov Protocol Registration and Results System (PRS) and is intended for newer PRS users who want to quickly get up to speed on PRS functions and best practices. Attendees will be given a guided tour of PRS features and learn key principles and approaches for submitting high quality registration and results information. To maximize practical application, instructors will draw on examples from real study submissions.
- Utilize the PRS Planning Report to identify studies in their PRS account that may require attention
- Discuss best practices for describing primary and secondary outcome measures
- Identify key informational resources that are intended to support the submission process