Ethics and etiquette in an emergency vaccine trial. The orchestration of compliance

Participant non-compliance and withdrawal from randomized clinical trials has increased focus on analysing the results from the “per-protocol” population that complies with a trial’s protocols. There is no clear understanding of what shapes protocol compliance in practice. In this paper, I theorize...

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Main Author: Arsenii Alenichev
Format: Article
Language:English
Published: Taylor & Francis Group 2020-01-01
Series:Global Bioethics
Subjects:
Online Access:http://dx.doi.org/10.1080/11287462.2020.1726591
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spelling doaj-d6c989cad7d0418885af650cc4f054122020-12-17T12:50:43ZengTaylor & Francis GroupGlobal Bioethics1128-74621591-73982020-01-01311132810.1080/11287462.2020.17265911726591Ethics and etiquette in an emergency vaccine trial. The orchestration of complianceArsenii Alenichev0Department of Anthropology, University of AmsterdamParticipant non-compliance and withdrawal from randomized clinical trials has increased focus on analysing the results from the “per-protocol” population that complies with a trial’s protocols. There is no clear understanding of what shapes protocol compliance in practice. In this paper, I theorize clinical research from the perspective of participants in an Ebola vaccine trial by analysing the practices that contributed to very high compliance rates. In this setting, per-protocol compliance became an essential component in forming a class of “proper” researchers and participants working together in the rapidly expanding market of clinical research. Bioethics supports participants’ right to withdraw from research as an ethical safeguard in the process. But participants seeking affiliations with powerful institutions may voluntarily embrace their trial responsibilities over a right to withdraw. To understand this phenomenon, this analysis uses the notion of bioetiquette – the set of rules specifying “proper” and “improper” trial subjects and behaviours – which runs in the shadow of formal bioethics in trials and requires careful transdisciplinary examination.http://dx.doi.org/10.1080/11287462.2020.1726591ebolaclinical trialsbioethicsbioetiquettecompliance
collection DOAJ
language English
format Article
sources DOAJ
author Arsenii Alenichev
spellingShingle Arsenii Alenichev
Ethics and etiquette in an emergency vaccine trial. The orchestration of compliance
Global Bioethics
ebola
clinical trials
bioethics
bioetiquette
compliance
author_facet Arsenii Alenichev
author_sort Arsenii Alenichev
title Ethics and etiquette in an emergency vaccine trial. The orchestration of compliance
title_short Ethics and etiquette in an emergency vaccine trial. The orchestration of compliance
title_full Ethics and etiquette in an emergency vaccine trial. The orchestration of compliance
title_fullStr Ethics and etiquette in an emergency vaccine trial. The orchestration of compliance
title_full_unstemmed Ethics and etiquette in an emergency vaccine trial. The orchestration of compliance
title_sort ethics and etiquette in an emergency vaccine trial. the orchestration of compliance
publisher Taylor & Francis Group
series Global Bioethics
issn 1128-7462
1591-7398
publishDate 2020-01-01
description Participant non-compliance and withdrawal from randomized clinical trials has increased focus on analysing the results from the “per-protocol” population that complies with a trial’s protocols. There is no clear understanding of what shapes protocol compliance in practice. In this paper, I theorize clinical research from the perspective of participants in an Ebola vaccine trial by analysing the practices that contributed to very high compliance rates. In this setting, per-protocol compliance became an essential component in forming a class of “proper” researchers and participants working together in the rapidly expanding market of clinical research. Bioethics supports participants’ right to withdraw from research as an ethical safeguard in the process. But participants seeking affiliations with powerful institutions may voluntarily embrace their trial responsibilities over a right to withdraw. To understand this phenomenon, this analysis uses the notion of bioetiquette – the set of rules specifying “proper” and “improper” trial subjects and behaviours – which runs in the shadow of formal bioethics in trials and requires careful transdisciplinary examination.
topic ebola
clinical trials
bioethics
bioetiquette
compliance
url http://dx.doi.org/10.1080/11287462.2020.1726591
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