Ethical Acceptability of Postrandomization Consent in Pragmatic Clinical Trials

IMPORTANCE: Pragmatic clinical trials that seek informed consent after randomization (ie, postrandomization consent) are increasingly used, but debate on ethics persists because control arm patients are not specifically informed about the trials and randomization occurs before consent for the trials...

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Detalles Bibliográficos
Autores principales: Miller, David Gibbes, Kim, Scott Y. H., Li, Xiaobai, Dickert, Neal W., Flory, James, Runge, Carlisle P., Relton, Clare
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2018
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324565/
https://www.ncbi.nlm.nih.gov/pubmed/30646316
http://dx.doi.org/10.1001/jamanetworkopen.2018.6149

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6324565/
https://www.ncbi.nlm.nih.gov/pubmed/30646316
http://dx.doi.org/10.1001/jamanetworkopen.2018.6149

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