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Informed consent: time for more transparency
Informed 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...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911861/ https://www.ncbi.nlm.nih.gov/pubmed/20537202 http://dx.doi.org/10.1186/ar3004 |
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author | Yazici, Yusuf Yazici, Hasan |
author_facet | Yazici, Yusuf Yazici, Hasan |
author_sort | Yazici, Yusuf |
collection | PubMed |
description | Informed 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. |
format | Text |
id | pubmed-2911861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29118612010-12-03 Informed consent: time for more transparency Yazici, Yusuf Yazici, Hasan Arthritis Res Ther Commentary Informed 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. BioMed Central 2010 2010-06-03 /pmc/articles/PMC2911861/ /pubmed/20537202 http://dx.doi.org/10.1186/ar3004 Text en Copyright ©2010 BioMed Central Ltd |
spellingShingle | Commentary Yazici, Yusuf Yazici, Hasan Informed consent: time for more transparency |
title | Informed consent: time for more transparency |
title_full | Informed consent: time for more transparency |
title_fullStr | Informed consent: time for more transparency |
title_full_unstemmed | Informed consent: time for more transparency |
title_short | Informed consent: time for more transparency |
title_sort | informed consent: time for more transparency |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911861/ https://www.ncbi.nlm.nih.gov/pubmed/20537202 http://dx.doi.org/10.1186/ar3004 |
work_keys_str_mv | AT yaziciyusuf informedconsenttimeformoretransparency AT yazicihasan informedconsenttimeformoretransparency |