Patient and Proxy Recall After Providing Written or Oral Informed Consent to Participate in an Interventional Trial

This cohort study assesses recall rates among patients and their proxies who consented to participate in a randomized clinical trial.

Detalles Bibliográficos
Autores principales: Huttner, Angela, von Dach, Elodie, Prendki, Virginie, Harbarth, Stephan, Kaiser, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2022
Materias:
Research Letter
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9107023/
https://www.ncbi.nlm.nih.gov/pubmed/35560052
http://dx.doi.org/10.1001/jamanetworkopen.2022.14052

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9107023/
https://www.ncbi.nlm.nih.gov/pubmed/35560052
http://dx.doi.org/10.1001/jamanetworkopen.2022.14052

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