Protocol SmartDesign: Data-Backed Recommendations For Primary Endpoints And I/E Criteria

Protocol SmartDesign is an AI-powered tool from Citeline that helps streamline clinical trial protocol design. It leverages data from Sitetrove and Trialtrove, considered the gold standard in clinical trial data, to generate data-backed recommendations for primary endpoints and inclusion/exclusion criteria.

This brochure details several features of Protocol SmartDesign that assist clinical trial teams throughout the process. It analyzes vast datasets (including 750,000+ trials) while providing granular detail on the source information for each recommendation, allowing for transparency and informed decision-making. The platform facilitates collaboration by enabling teams to share protocols in a centralized location. Additionally, Protocol SmartDesign leverages historical data to forecast trial duration. The tool also allows for real-time updates to inclusion/exclusion criteria, with automatic adjustments to the forecasted enrollment rate and trial duration. 

Overall, Protocol SmartDesign offers a data-driven approach to clinical trial protocol design to improve predictability and efficiency throughout the trial process.