Clinical Trials on Adverse Drug Reactions: An In-Depth Analysis Using ClinicalTrials.gov Database
Presentation
Overview
Overview
Description
Understanding adverse drug reactions (ADRs) during clinical trials is critical for enhancing trial design and identifying under-researched areas. Increased awareness of drug safety concerns have driven improvements in the design and reporting of ADR-related trials over time. This study aims to provide an inclusive analysis of ADR focused clinical trials registered in the ClinicalTrials.gov database.
