Which factors influence the resort to surrogate consent in stroke trials, and what are the patient outcomes in this context?

BACKGROUND: The provision of informed consent is a prerequisite for inclusion of a patient in a clinical research project. In some countries, the legislation on clinical research authorizes a third person to provide informed consent if the patient is unable to do so directly (i.e. surrogate consent)...

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Detalles Bibliográficos
Autores principales: Mendyk, Anne-Marie, Labreuche, Julien, Henon, Hilde, Girot, Marie, Cordonnier, Charlotte, Duhamel, Alain, Leys, Didier, Bordet, Régis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415257/
https://www.ncbi.nlm.nih.gov/pubmed/25903471
http://dx.doi.org/10.1186/s12910-015-0018-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415257/
https://www.ncbi.nlm.nih.gov/pubmed/25903471
http://dx.doi.org/10.1186/s12910-015-0018-8

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