Safety reporting in trials on glaucoma interventions registered in ClinicalTrials.gov and corresponding publications

Abstract Accurate, comprehensive, and consistent reporting of adverse events is of great importance for treatment decisions in clinical practice and patient safety. Aiming to evaluate the completeness and transparency of reported adverse events we conducted a retrospective analysis of completed clin...

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Bibliographic Details

Published in:	Scientific Reports
Main Authors:	Ante Krešo, Marko Grahovac, Ljubo Znaor, Ana Marušić
Format:	Article
Language:	English
Published:	Nature Portfolio 2024-11-01
Subjects:	Glaucoma treatment Reporting Adverse event Harms Safety ClinicalTrials.gov
Online Access:	https://doi.org/10.1038/s41598-024-79394-z