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Patients’ beliefs regarding informed consent for low-risk pragmatic trials

BACKGROUND: The requirement to obtain written informed consent may undermine the potential of pragmatic randomized clinical trials (pRCTs) to improve evidence-based care. This requirement could compromise trials statistical power or even force it to close them down prematurely. However, recent data...

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Detalles Bibliográficos
Autores principales:	Dal-Ré, Rafael, Carcas, Antonio J., Carné, Xavier, Wendler, David
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2017
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5604493/ https://www.ncbi.nlm.nih.gov/pubmed/28923007 http://dx.doi.org/10.1186/s12874-017-0424-3

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