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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Bibliographic Details
Main Authors: Maria López-Parra, Francesc Zamora-Carmona, Mònica Sianes-Gallén, Esmeralda López-González, Dolors Gil-Rey, Helena Costa-Ventura, Miriam Borrás-Sánchez, Gemma Rayo-Posadas, Marta Arizu-Puigvert, Roser Vives-Vilagut
Format: Article
Language:English
Published: MDPI AG 2022-06-01
Series:Healthcare
Subjects:
Online Access:https://www.mdpi.com/2227-9032/10/6/1036