Informed consent for clinical trials in acute coronary syndromes and stroke following the European Clinical Trials Directive: investigators' experiences and attitudes

BACKGROUND: During clinical trials in emergency medicine, providing appropriate oral and written information to a patient is usually a challenge. There is little published information regarding patients' opinions and competence to provide informed consent, nor on physicians' attitudes towa...

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Detalles Bibliográficos
Autores principales: Iwanowski, Piotr, Budaj, Andrzej, Członkowska, Anna, Wąsek, Wojciech, Kozłowska-Boszko, Beata, Olędzka, Urszula, Masełbas, Wojciech
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2517587/
https://www.ncbi.nlm.nih.gov/pubmed/18644120
http://dx.doi.org/10.1186/1745-6215-9-45

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2517587/
https://www.ncbi.nlm.nih.gov/pubmed/18644120
http://dx.doi.org/10.1186/1745-6215-9-45

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