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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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Detalhes bibliográficos
Publicado no:Br J Clin Pharmacol
Main Authors: Dal‐Ré, Rafael, Carcas, Antonio J., Carné, Xavier, Wendler, David
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2017
Assuntos:
Acesso em linha: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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