Participant informed consent in cluster randomized trials: review.

<h4>Background</h4>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...

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Autores principales: Bruno Giraudeau, Agnès Caille, Amélie Le Gouge, Philippe Ravaud
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2012
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Acceso en línea:https://doaj.org/article/4fb9ea9bcc9a4c118d5d1d9ec3c0d586
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