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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cancer Intelligence
2014
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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 |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-3894239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cancer Intelligence |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT nardinicecilia theethicsofclinicaltrials AT nardinicecilia ethicsofclinicaltrials |