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dc.rights.licenseEscolha o acesso:::ACESSO ABERTO (CC BY-NC-ND 4.0) - A Regulação Autoral da Biblioteca Digital da Anvisa permite o reconhecimento da produção intelectual como sendo de acesso aberto, adotando-se assim, a Creative Commons Attribution-NonCommercial-NonDerivates 4.0 International. Concedendo a outros que realizem o download e compartilhamento da produção intelectual desde que atribuam crédito ao autor, mas sem que possam alterá-los de nenhuma forma ou utilizá-los para fins comerciais.pt_BR
dc.contributor.authorSilva, Ricardo E. da-
dc.contributor.authorAmato, Angélica A.-
dc.contributor.authorGuilhem, Dirce B.-
dc.contributor.authorCarvalho, Marta R. de-
dc.contributor.authorLima, Elisangela da C.-
dc.contributor.authorNovaes, Maria Rita C. G.-
dc.date.accessioned2022-09-06T18:11:21Z-
dc.date.available2022-09-06T18:11:21Z-
dc.date.issued2018-01-17-
dc.identifier.issn1663-9812-
dc.identifier.urihttp://bibliotecadigital.anvisa.ibict.br/jspui/handle/anvisa/1684-
dc.description.abstractBackground: 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.pt_BR
dc.language.isoenpt_BR
dc.titleFactors contributing to exacerbating vulnerabilities in global clinical trialspt_BR
dc.typeArtigopt_BR
dc.rights.holderRicardo E. da Silvapt_BR
dc.rights.holderAngélica A. Amatopt_BR
dc.rights.holderDirce B. Guilhempt_BR
dc.rights.holderMarta R. de Carvalhopt_BR
dc.rights.holderElisangela da C. Limapt_BR
dc.rights.holderMaria Rita C. G. Novaespt_BR
dc.identifier.doihttps://doi.org/10.3389/fphar.2017.00999-
dc.local[Lausanne]pt_BR
dc.description.physical10 p.pt_BR
dc.description.additionalReceived: 15 September 2017 -- Accepted: 28 December 2017 -- Published: 17 January 2018pt_BR
dc.description.additionalComo citar: SILVA, Ricardo E. da; AMATO, Angélica A.; GUILHEM, Dirce B.; CARVALHO, Marta R. de; LIMA, Elisangela da C.; NOVAES, Maria Rita C. G. Factors contributing to exacerbating vulnerabilities in global clinical trials. Frontiers in Pharmacology, [Lausanne], v. 8, article 999, January 2018. DOI 10.3389/fphar.2017.00999. Disponível em: https://www.frontiersin.org/articles/10.3389/fphar.2017.00999/full. Acesso em: 6 set. 2022.pt_BR
dc.subject.keywordClinical trialspt_BR
dc.subject.keywordVulnerable populationpt_BR
dc.subject.keywordVulnerabilitypt_BR
dc.subject.keywordSocioeconomic statuspt_BR
dc.subject.keywordENSAIOS CLÍNICOSpt_BR
dc.subject.keywordPopulação vulnerávelpt_BR
dc.subject.keywordVulnerabilidadept_BR
dc.subject.keywordStatus socioeconômicopt_BR
dc.rights.accessAcesso Abertopt_BR
dc.itemdestaqueNãopt_BR
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