Lack of transparent reporting of trial monitoring approaches in randomised controlled trials: A systematic review of contemporary protocol papers

BACKGROUND: Monitoring is essential to ensure patient safety and data integrity in clinical trials as per Good Clinical Practice. The Standard Protocol Items: Recommendations for Interventional Trials Statement and its checklist guides authors to include monitoring in their protocols. We investigate...

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Detalles Bibliográficos
Autores principales: Hsieh, Shao-Fan, Yorke-Edwards, Victoria, Murray, Macey L, Diaz-Montana, Carlos, Love, Sharon B, Sydes, Matthew R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10021127/
https://www.ncbi.nlm.nih.gov/pubmed/36629015
http://dx.doi.org/10.1177/17407745221143449

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10021127/
https://www.ncbi.nlm.nih.gov/pubmed/36629015
http://dx.doi.org/10.1177/17407745221143449

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