How informed is consent in vulnerable populations? Experience using a continuous consent process during the MDP301 vaginal microbicide trial in Mwanza, Tanzania

BACKGROUND: HIV prevention trials conducted among disadvantaged vulnerable at-risk populations in developing countries present unique ethical dilemmas. A key concern in bioethics is the validity of informed consent for trial participation obtained from research subjects in such settings. The purpose...

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Detalles Bibliográficos
Autores principales: Vallely, Andrew, Lees, Shelley, Shagi, Charles, Kasindi, Stella, Soteli, Selephina, Kavit, Natujwa, Vallely, Lisa, McCormack, Sheena, Pool, Robert, Hayes, Richard J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2893460/
https://www.ncbi.nlm.nih.gov/pubmed/20540803
http://dx.doi.org/10.1186/1472-6939-11-10

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2893460/
https://www.ncbi.nlm.nih.gov/pubmed/20540803
http://dx.doi.org/10.1186/1472-6939-11-10

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