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Public preferences on written informed consent for low‐risk pragmatic clinical trials in Spain

AIMS: Pragmatic randomized clinical trials (pRCTs) collect data that have the potential to improve medical care significantly. However, these trials may be undermined by the requirement to obtain written informed consent, which can decrease accrual and increase selection bias. Recent data suggest th...

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Detalles Bibliográficos
Publicado en:Br J Clin Pharmacol
Main Authors: Dal‐Ré, Rafael, Carcas, Antonio J., Carné, Xavier, Wendler, David
Formato: Artigo
Idioma:Inglês
Publicado: John Wiley and Sons Inc. 2017
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5582372/
https://ncbi.nlm.nih.gov/pubmed/28419518
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bcp.13305
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