Attitudes Toward Risk and Informed Consent for Research on Medical Practices: A Cross-sectional Survey

BACKGROUND: The U.S. Office for Human Research Protections has proposed that end points of randomized trials comparing the effectiveness of standard medical practices are risks of research that would require disclosure and written informed consent, but data are lacking on the views of potential part...

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Publicado en:Ann Intern Med
Autores principales: Cho, Mildred K., Magnus, David, Constantine, Melissa, Lee, Sandra Soo-Jin, Kelley, Maureen, Alessi, Stephanie, Korngiebel, Diane, James, Cyan, Kuwana, Ellen, Gallagher, Thomas H., Diekema, Douglas, Capron, Alexander M., Joffe, Steven, Wilfond, Benjamin S.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2015
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4776759/
https://ncbi.nlm.nih.gov/pubmed/25868119
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7326/M15-0166
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