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)...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:BMC Med Ethics
Autors principals: Mendyk, Anne-Marie, Labreuche, Julien, Henon, Hilde, Girot, Marie, Cordonnier, Charlotte, Duhamel, Alain, Leys, Didier, Bordet, Régis
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2015
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4415257/
https://ncbi.nlm.nih.gov/pubmed/25903471
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12910-015-0018-8
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars