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...
Gardado en:
| Publicado en: | BMJ |
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| Principais autores: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BMJ Publishing Group
2003
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC166125/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12881261/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/bmj.327.7408.198 |
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