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Participant Informed Consent in Cluster Randomized Trials: Review

BACKGROUND: The Nuremberg code defines the general ethical framework of medical research with participant consent as its cornerstone. In cluster randomized trials (CRT), obtaining participant informed consent raises logistic and methodologic concerns. First, with randomization of large clusters such...

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Detalhes bibliográficos
Main Authors: Giraudeau, Bruno, Caille, Agnès, Le Gouge, Amélie, Ravaud, Philippe
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3391275/
https://ncbi.nlm.nih.gov/pubmed/22792319
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0040436
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