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Factors Contributing to Exacerbating Vulnerabilities in Global Clinical Trials
Background: Although policies and guidelines make use of the concept of vulnerability, few define it. The European Union's directive for clinical trials does not include explanations for or the reasoning behind the designation of certain groups as vulnerable. Emerging economies from lower middl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776907/ https://www.ncbi.nlm.nih.gov/pubmed/29403381 http://dx.doi.org/10.3389/fphar.2017.00999 |
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author | da Silva, Ricardo E. Amato, Angélica A. Guilhem, Dirce B. de Carvalho, Marta R. Lima, Elisangela da C. Novaes, Maria Rita C. G. |
author_facet | da Silva, Ricardo E. Amato, Angélica A. Guilhem, Dirce B. de Carvalho, Marta R. Lima, Elisangela da C. Novaes, Maria Rita C. G. |
author_sort | da Silva, Ricardo E. |
collection | PubMed |
description | Background: Although policies and guidelines make use of the concept of vulnerability, few define it. The European Union's directive for clinical trials does not include explanations for or the reasoning behind the designation of certain groups as vulnerable. Emerging economies from lower middle-income countries have, in recent years, had the largest average annual growth rate, as well as increase, in number of clinical trials registered in the US government's database. Nevertheless, careful supervision of research activities has to be ensured. Objective: To describe and analyze the features of the clinical trials involving vulnerable populations in various countries classified by development status and geographic region. Methods: Retrospective study that involved analysis of data obtained from the International Clinical Trials Registry Platform (ICTRP) database between 01/2014 and 12/2014 from countries with (i) highest trial densities during 2005 to 2012, (ii) highest average growth rate in clinical trials, and (iii) greatest trial capabilities. Results: Statistical analysis of this study showed that patients incapable of giving consent personally are 11.4 times more likely to be vulnerable patients than patients who are capable, and that patients in upper-middle-income countries are 1.7 times more likely to be vulnerable patients than patients from high-income countries when participating in global clinical trials. Malaysia (21%), Egypt (20%), Turkey (19%), Israel (18%), and Brazil (17%) had the highest percentages of vulnerable populations involving children. Conclusions: Although the inability to provide consent personally was a factor associated with vulnerability, arbitrary criteria may have been considered when classifying the populations of clinical trials as vulnerable. The EU Clinical Trials Register should provide guidance regarding exactly what aspects or factors should be taken into account to frame given populations as vulnerable, because vulnerability is not applicable to all risk situations. |
format | Online Article Text |
id | pubmed-5776907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57769072018-02-05 Factors Contributing to Exacerbating Vulnerabilities in Global Clinical Trials da Silva, Ricardo E. Amato, Angélica A. Guilhem, Dirce B. de Carvalho, Marta R. Lima, Elisangela da C. Novaes, Maria Rita C. G. Front Pharmacol Pharmacology Background: Although policies and guidelines make use of the concept of vulnerability, few define it. The European Union's directive for clinical trials does not include explanations for or the reasoning behind the designation of certain groups as vulnerable. Emerging economies from lower middle-income countries have, in recent years, had the largest average annual growth rate, as well as increase, in number of clinical trials registered in the US government's database. Nevertheless, careful supervision of research activities has to be ensured. Objective: To describe and analyze the features of the clinical trials involving vulnerable populations in various countries classified by development status and geographic region. Methods: Retrospective study that involved analysis of data obtained from the International Clinical Trials Registry Platform (ICTRP) database between 01/2014 and 12/2014 from countries with (i) highest trial densities during 2005 to 2012, (ii) highest average growth rate in clinical trials, and (iii) greatest trial capabilities. Results: Statistical analysis of this study showed that patients incapable of giving consent personally are 11.4 times more likely to be vulnerable patients than patients who are capable, and that patients in upper-middle-income countries are 1.7 times more likely to be vulnerable patients than patients from high-income countries when participating in global clinical trials. Malaysia (21%), Egypt (20%), Turkey (19%), Israel (18%), and Brazil (17%) had the highest percentages of vulnerable populations involving children. Conclusions: Although the inability to provide consent personally was a factor associated with vulnerability, arbitrary criteria may have been considered when classifying the populations of clinical trials as vulnerable. The EU Clinical Trials Register should provide guidance regarding exactly what aspects or factors should be taken into account to frame given populations as vulnerable, because vulnerability is not applicable to all risk situations. Frontiers Media S.A. 2018-01-17 /pmc/articles/PMC5776907/ /pubmed/29403381 http://dx.doi.org/10.3389/fphar.2017.00999 Text en Copyright © 2018 Silva, Amato, Guilhem, Carvalho, Lima and Novaes. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology da Silva, Ricardo E. Amato, Angélica A. Guilhem, Dirce B. de Carvalho, Marta R. Lima, Elisangela da C. Novaes, Maria Rita C. G. Factors Contributing to Exacerbating Vulnerabilities in Global Clinical Trials |
title | Factors Contributing to Exacerbating Vulnerabilities in Global Clinical Trials |
title_full | Factors Contributing to Exacerbating Vulnerabilities in Global Clinical Trials |
title_fullStr | Factors Contributing to Exacerbating Vulnerabilities in Global Clinical Trials |
title_full_unstemmed | Factors Contributing to Exacerbating Vulnerabilities in Global Clinical Trials |
title_short | Factors Contributing to Exacerbating Vulnerabilities in Global Clinical Trials |
title_sort | factors contributing to exacerbating vulnerabilities in global clinical trials |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776907/ https://www.ncbi.nlm.nih.gov/pubmed/29403381 http://dx.doi.org/10.3389/fphar.2017.00999 |
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