Which factors influence the resort to surrogate consent in stroke trials, and what are the patient o...
Which factors influence the resort to surrogate consent in stroke trials, and what are the patient outcomes in this context?
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Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Contents
The provision of informed consent is a prerequisite for inclusion of a patient in a clinical research project. In some countries, the legislation on clinical research authorizes a third person to provide informed consent if the patient is unable to do so directly (i.e. surrogate consent). This is the case during acute stroke, when the symptoms may...
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Full title
Which factors influence the resort to surrogate consent in stroke trials, and what are the patient outcomes in this context?
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4415257
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4415257
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ISSN
1472-6939
E-ISSN
1472-6939
DOI
10.1186/s12910-015-0018-8
