9 found
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  1.  14
    A Trust‐Based Pact in Research Biobanks. From Theory to Practice.Virginia Sanchini, Giuseppina Bonizzi, Davide Disalvatore, Massimo Monturano, Salvatore Pece, Giuseppe Viale, Pier Paolo Di Fiore & Giovanni Boniolo - 2016 - Bioethics 30 (4):260-271.
    Traditional Informed Consent is becoming increasingly inadequate, especially in the context of research biobanks. How much information is needed by patients for their consent to be truly informed? How does the quality of the information they receive match up to the quality of the information they ought to receive? How can information be conveyed fairly about future, non-predictable lines of research? To circumvent these difficulties, some scholars have proposed that current consent guidelines should be reassessed, with trust being used as (...)
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  2.  21
    Informed Consent as an Ethical Requirement in Clinical Trials: An Old, but Still Unresolved Issue. An Observational Study to Evaluate Patient's Informed Consent Comprehension.Virginia Sanchini, Michele Reni, Giliola Calori, Elisabetta Riva & Massimo Reichlin - 2014 - Journal of Medical Ethics 40 (4):269-275.
    We explored the comprehension of the informed consent in 77 cancer patients previously enrolled in randomised phase II or phase III clinical trials, between March and July 2011, at the San Raffaele Scientific Institute in Milano. We asked participants to complete an ad hoc questionnaire and analysed their answers. Sixty-two per cent of the patients understood the purpose and nature of the trial they were participating in; 44% understood the study procedures and 40% correctly listed at least one of the (...)
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  3.  19
    Potential Pitfalls in the Evaluation of Ethics Consultation: The Case of Ethical Counseling.Alma Linkeviciute, Kris Dierickx, Virginia Sanchini & Giovanni Boniolo - 2016 - American Journal of Bioethics 16 (3):56-57.
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  4.  39
    The Ethics of Non-Inferiority Trials: A Consequentialist Analysis.Marco Annoni, Virginia Sanchini & Cecilia Nardini - 2013 - Research Ethics 9 (3):109-120.
    Discussions about the merits and shortcomings of non-inferiority trials are becoming increasingly common in the medical community and among regulatory agencies. However, criticisms targeting the ethical standing of non-inferiority trials have often been mistargeted. In this article we review the ethical standing of trials of non-inferiority. In the first part of the article, we outline a consequentialist position according to which clinical trials are best conceived as epistemic tools aimed at fostering the proper ends of medicine. According to this view, (...)
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  5.  14
    L’allocazione delle risorse sanitarie durante la pandemia da Covid-19: un’analisi comparativa dei documenti della SIAARTI e del CNB.Davide Battisti, Luca Marelli, Mario Picozzi, Massimo Reichlin & Virginia Sanchini - 2021 - Notizie di Politeia 141:25-45.
    In Italy, during the first wave of the Covid-19 pandemic, the Italian Society of Resuscitators and Pain Therapists (SIAARTI) and the Italian National Bioethics Committee (CNB) published ethical guidance on the allocation of scarce intensive care resources. In this paper, we outline and compare these documents in detail, highlighting differences and similarities. In particular, we argue that major differences exist with respect to the principles and values underpinning the documents and the normative allocation criteria proposed. Conversely, similarities can be traced (...)
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  6.  3
    Imagining Human Reproduction. Introduction: Imagining Human Reproduction.Simona Corso, Florian Mussgnug & Virginia Sanchini - 2020 - Phenomenology and Mind 19:12.
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  7.  10
    Evaluating the Effectiveness of Clinical Ethics Committees: A Systematic Review.Chiara Crico, Virginia Sanchini, Paolo Giovanni Casali & Gabriella Pravettoni - 2021 - Medicine, Health Care and Philosophy 24 (1):135-151.
    Clinical Ethics Committees, as distinct from Research Ethics Committees, were originally established with the aim of supporting healthcare professionals in managing controversial clinical ethical issues. However, it is still unclear whether they manage to accomplish this task and what is their impact on clinical practice. This systematic review aims to collect available assessments of CECs’ performance as reported in literature, in order to evaluate CECs’ effectiveness. We retrieved all literature published up to November 2019 in six databases, following PRISMA guidelines. (...)
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  8.  6
    Ethics Review in Anti-Doping Research: Experiences of Stakeholders.Thijs Devriendt, Virginia Sanchini & Pascal Borry - 2020 - Ajob Empirical Bioethics 11 (2):125-133.
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  9.  2
    Deliberation and Public Bioethics: A Test Case in Reproductive Genetics.Virginia Sanchini, Davide Disalvatore, Sarah Songhorian, Paolo Spada & Pier Paolo Di Fiore - 2020 - Phenomenology and Mind 19:150.
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