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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Bibliographic Details
Main Authors: Bruno Giraudeau, Agnès Caille, Amélie Le Gouge, Philippe Ravaud
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22792319/pdf/?tool=EBI

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