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Improving the capture and reporting of adverse events in clinical trials of non-pharmacological interventions: learnings from the PaCCSC/CST membership

Abstract Background Accurate capture and reporting of adverse events (AEs) in clinical trials is critical to understanding the potential harms of prospective interventions. Current AE-reporting frameworks are specifically constructed for pharmacological interventions and adaptation of these framewor...

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Principais autores: Rayan Saleh Moussa, Jack Power, Vanessa Yenson, Belinda Fazekas, Celia Marston, Annmarie Hosie, Layla Edwards, Domenica Disalvo, Linda Brown, Imelda Gilmore, John Stubbs, Andrea Cross, Sally Fielding, Meera R. Agar
Formato: Artigo
Idioma:Inglês
Publicado em: BMC 2025-03-01
coleção:Trials
Assuntos:
Adverse events
Non-pharmacological
Risk management
Clinical trials
Intervention
Harm
Acesso em linha:https://doi.org/10.1186/s13063-025-08801-1
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