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Informed consent in trials for neurological emergencies: the example of subarachnoid haemorrhage

Objectives: To assess what relevant information could be recalled by patients who were living independently after a subarachnoid haemorrhage, and by their relatives; and to determine how these patients and relatives had reacted to the informed consent encounter. Methods: Twenty months (range 7 to 31...

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Bibliografiska uppgifter
Huvudupphovsmän: Schats, R, Brilstra, E, Rinkel, G, Algra, A, van Gijn, J
Materialtyp: Artigo
Språk:Inglês
Publicerad: BMJ Group 2003
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1738516/
https://ncbi.nlm.nih.gov/pubmed/12810803
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.74.7.988
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