Zobrazeno 1 - 5
of 5
pro vyhledávání: '"MESH: Consent"'
Autor:
Delafoy, Élodie
Publikováno v:
Gynécologie et obstétrique. 2017
Objective: the objectives of this study are to know which informations about episiotomy are communicated to patients according to them and to understand the influence of this data on their acceptance of the gesture. Methods: It is a qualitative study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::219549b10d3dc1e466fc21a5a629f2ea
https://dumas.ccsd.cnrs.fr/dumas-01585485/file/memoire_esfbaudelocque_delafoy.pdf
https://dumas.ccsd.cnrs.fr/dumas-01585485/file/memoire_esfbaudelocque_delafoy.pdf
Autor:
Pot, Anne-Louise
Publikováno v:
Médecine humaine et pathologie. 2015
Psychiatry is a medical discipline characterized by psychically weakening diseases, and alegislation about the hospitalization of patients.Health Law of March 4th 2002 introduces the possibility for all patients, without distinction forpsychiatry, to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0cb5245510867c3505bb1ae90cf0b081
https://dumas.ccsd.cnrs.fr/dumas-01252522
https://dumas.ccsd.cnrs.fr/dumas-01252522
Autor:
Paris , Adeline, Cracowski , Jean-Luc, Ravanel , Nadia, Cornu , Catherine, Gueyffier , François, Deygas , Béatrice, Guillot , Karine, Bosson , Jean-Luc, Hommel , Marc
Publikováno v:
La Presse Médicale
La Presse Médicale, Elsevier Masson, 2005, 34 (1), pp.13-8
La Presse Médicale, Elsevier Masson, 2005, 34 (1), pp.13-8
National audience; OBJECTIVE: We compared informed consent forms of subjects participating in biomedical research with those of references texts in order to determine the factors that influence readability. METHODS: We assessed the readability of 73
Autor:
Sabina Gainotti, Pierre Durieux, Isabelle Durand-Zaleski, Ph Ravaud, X. Duval, Philippe Amiel, Serge Gottot, Delphine Moreau, Corinne Alberti, Claire Vincent-Genod
Publikováno v:
Journal of Medical Ethics
Journal of Medical Ethics, BMJ Publishing Group, 2008, 34 (9), pp.e16. ⟨10.1136/jme.2007.023473⟩
Journal of Medical Ethics, 2008, 34 (9), pp.e16. ⟨10.1136/jme.2007.023473⟩
Journal of Medical Ethics, BMJ Publishing Group, 2008, 34 (9), pp.e16. ⟨10.1136/jme.2007.023473⟩
Journal of Medical Ethics, 2008, 34 (9), pp.e16. ⟨10.1136/jme.2007.023473⟩
International audience; BACKGROUND: Informed consent in clinical research is mandated throughout the world. Both patient subjects and investigators are required to understand and accept the distinction between research and treatment. AIM: To document
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63fdde7f82ea6b43f983341451911641
https://hal.archives-ouvertes.fr/hal-00850486
https://hal.archives-ouvertes.fr/hal-00850486
Autor:
Adeline Paris, Jean-Luc Cracowski, Christophe Ribuot, Catherine Cornu, Muriel Salvat-Melis, Jean-Luc Bosson, Christian Brandt, Daniel Nogueira da Gama Chaves, Marc Hommel, Patrick Maison
Publikováno v:
Fundamental and Clinical Pharmacology
Fundamental and Clinical Pharmacology, Wiley, 2007, 21 (2), pp.207-14. ⟨10.1111/j.1472-8206.2007.00472.x⟩
Fundamental and Clinical Pharmacology, Wiley, 2007, 21 (2), pp.207-14. ⟨10.1111/j.1472-8206.2007.00472.x⟩
Writing an informed consent form (ICF) for biomedical research is a difficult task. We conducted a multicenter single-blind randomized controlled trial to identify whether a working group or the systematic improvement in lexico-syntactic readability
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97e8d955aa9a6031b2c0cc8a0993a882
https://hal.archives-ouvertes.fr/hal-00281336
https://hal.archives-ouvertes.fr/hal-00281336