Article

MedDRA Adoption and Adverse Event Reporting Quality in Gastrointestinal and Abdominal Surgery Randomized Controlled Trials: A Cross-Sectional Analysis

2026-02-05

Abstract excerpt

<h4>ABSTRACT</h4> <h4>Introduction</h4> Adverse event (AE) reporting transparency is essential for evidence-based surgical practice, yet substantial reporting gaps persist despite Consolidated Standards for Reporting Trials (CONSORT) Harms guidance. The Medical Dictionary for Regulatory Activities (MedDRA) provides standardized terminology for AE classification, but its association with AE reporting quality rema...

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Literature Corpus work: d09c7146-5b86-5772-b07a-d0420051d0d7
DOI: 10.64898/2026.02.04.26345608

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