Patient Information and Informed Consent for Research in the Elderly: Lessons Learned from a Randomized Controlled Trial

The informed consent (IC) of subjects participating in experimental studies is the mainstay to comply with the ethical principle of autonomy to ensure that the participation is voluntary. This experience was performed within the context of a single-center randomized clinical trial in elective prosth...

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Detalles Bibliográficos
Autores principales: López-Parra, Maria, Zamora-Carmona, Francesc, Sianes-Gallén, Mònica, López-González, Esmeralda, Gil-Rey, Dolors, Costa-Ventura, Helena, Borrás-Sánchez, Miriam, Rayo-Posadas, Gemma, Arizu-Puigvert, Marta, Vives-Vilagut, Roser
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222813/
https://www.ncbi.nlm.nih.gov/pubmed/35742087
http://dx.doi.org/10.3390/healthcare10061036

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222813/
https://www.ncbi.nlm.nih.gov/pubmed/35742087
http://dx.doi.org/10.3390/healthcare10061036

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