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Novel consent process for research in dying patients unable to give consent

Objectives To develop a process of advance consent to enable research to be undertaken in patients in the terminal phase. Design Feasibility study of an advance consent process to support a randomised controlled trial of two antimuscarinic drugs (hyoscine hydrobromide and glycopyrronium bromide) in...

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Detalhes bibliográficos
Main Authors: Rees, Elizabeth, Hardy, Janet
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Publishing Group Ltd. 2003
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC166125/
https://ncbi.nlm.nih.gov/pubmed/12881261
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