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The ethics of clinical trials

Over the past decades, randomised controlled trials (RCTs) have prevailed over clinical judgement, case reports, and observational studies and became the gold evidential standard in medicine. Furthermore, during the same time frame, RCTs became a crucial part of the regulatory process whereby a new...

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Detalles Bibliográficos
Autor principal: Nardini, Cecilia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894239/
https://www.ncbi.nlm.nih.gov/pubmed/24482672
http://dx.doi.org/10.3332/ecancer.2014.387
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author Nardini, Cecilia
author_facet Nardini, Cecilia
author_sort Nardini, Cecilia
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description Over the past decades, randomised controlled trials (RCTs) have prevailed over clinical judgement, case reports, and observational studies and became the gold evidential standard in medicine. Furthermore, during the same time frame, RCTs became a crucial part of the regulatory process whereby a new therapeutic can gain access to the drug market. Today, clinical trials are large and tightly regulated enterprises that have to comply with ethical requirements while maintaining high epistemic standards, a balance that becomes increasingly difficult as the research questions become more sophisticated. In this review, the author will discuss some of the most important ethical issues surrounding RCTs, with an eye to the most recent debates and the context of oncological research in particular.
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spelling pubmed-38942392014-01-30 The ethics of clinical trials Nardini, Cecilia Ecancermedicalscience Review Over the past decades, randomised controlled trials (RCTs) have prevailed over clinical judgement, case reports, and observational studies and became the gold evidential standard in medicine. Furthermore, during the same time frame, RCTs became a crucial part of the regulatory process whereby a new therapeutic can gain access to the drug market. Today, clinical trials are large and tightly regulated enterprises that have to comply with ethical requirements while maintaining high epistemic standards, a balance that becomes increasingly difficult as the research questions become more sophisticated. In this review, the author will discuss some of the most important ethical issues surrounding RCTs, with an eye to the most recent debates and the context of oncological research in particular. Cancer Intelligence 2014-01-16 /pmc/articles/PMC3894239/ /pubmed/24482672 http://dx.doi.org/10.3332/ecancer.2014.387 Text en © the authors; licensee ecancermedicalscience. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Nardini, Cecilia
The ethics of clinical trials
title The ethics of clinical trials
title_full The ethics of clinical trials
title_fullStr The ethics of clinical trials
title_full_unstemmed The ethics of clinical trials
title_short The ethics of clinical trials
title_sort ethics of clinical trials
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894239/
https://www.ncbi.nlm.nih.gov/pubmed/24482672
http://dx.doi.org/10.3332/ecancer.2014.387
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