Informed consent in clinical research: do patients understand what they have signed?

Autor: Elena Villamañán, Margarita Ruano, Enma Fernández-de Uzquiano, Paz Lavilla, Diana González, Mercedes Freire, Carmen Sobrino, Alicia Herrero

Publikováno v: Farmacia Hospitalaria v.40 n.3 2016
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
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Farmacia Hospitalaria, Vol 40, Iss 3, Pp 209-218 (2016)

Informed consent is an essential element of research, and signing this document is required to conduct most clinical trials. Its aim is to inform patients what their participation in the study will involve. However, increasingly, their complexity and

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