Use of deferred consent for severely ill children in a multi-centre phase III trial

BACKGROUND: Voluntary participation of a subject in research respects a subject's rights, strengthens its ethical conduct, and is formalized by the informed consent process. Clinical trials of life-saving interventions for medical emergencies often necessitate enrolment of patients where prior...

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Detalles Bibliográficos
Autores principales: Maitland, Kathryn, Molyneux, Sassy, Boga, Mwamvua, Kiguli, Sarah, Lang, Trudie
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3077324/
https://www.ncbi.nlm.nih.gov/pubmed/21453454
http://dx.doi.org/10.1186/1745-6215-12-90

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3077324/
https://www.ncbi.nlm.nih.gov/pubmed/21453454
http://dx.doi.org/10.1186/1745-6215-12-90

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