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dc.contributor.authorYazici, Yusuf
dc.contributor.authorYazici, Hasan
dc.date.accessioned2021-03-06T09:01:57Z
dc.date.available2021-03-06T09:01:57Z
dc.date.issued2010
dc.identifier.citationYazici Y., Yazici H., "Informed consent: time for more transparency", ARTHRITIS RESEARCH & THERAPY, cilt.12, 2010
dc.identifier.issn1478-6354
dc.identifier.othervv_1032021
dc.identifier.otherav_e3d25a2f-ad5a-4354-9d0f-c667f46ba41c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/149897
dc.identifier.urihttps://doi.org/10.1186/ar3004
dc.description.abstractInformed consent is not only for documenting a patient's acceptance of enrolling in a clinical trial. It currently is the patient's and, we propose, should also be the public's main source of information regarding the reasons for the planned study, what is known in the field about the proposed trial, and what to expect as far as efficacy and harm. Informed consent is not currently part of the clinical trial registries. For purposes of full disclosure to the patients and the public, the informed consent should be part of the required documents for such registries.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectİmmünoloji ve Romatoloji
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titleInformed consent: time for more transparency
dc.typeMakale
dc.relation.journalARTHRITIS RESEARCH & THERAPY
dc.contributor.departmentCity University Of New York Brooklyn College , ,
dc.identifier.volume12
dc.identifier.issue3
dc.contributor.firstauthorID194737


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