Literature DB >> 23073901

Ethical aspects of clinical research with minors.

Wendy Bos1, Krista Tromp, Dick Tibboel, Wim Pinxten.   

Abstract

Over the past decades, clinical research has increasingly been subjected to ethical requirements and legal regulation. The specific focus of ethical and legal frameworks on competent adults (which serve as the paradigmatic research subject), however, has created an ambivalent attitude towards pediatric clinical research. On one hand, minors are regarded as a vulnerable population that deserves additional protection against the risks and burdens involved in clinical research. On the other hand, the population of minors should not be denied (or not get timely) access to the benefits of clinical research. In this paper, we will explore the legal regulation and ethical guidance that currently governs pediatric clinical research in the European Union and discuss the future challenges in this field. In addition, we will discuss major ethical concerns in pediatric clinical research, with a focus on the acceptability of research risks and the informed consent process. In the discussion, we will address key concerns in both regulating pediatric clinical research and implementing ethical and legal requirement in the actual pediatric research conduct.

Mesh:

Year:  2012        PMID: 23073901     DOI: 10.1007/s00431-012-1856-8

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  28 in total

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Authors:  Paul S Appelbaum; Charles W Lidz; Thomas Grisso
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2.  Therapeutic misconception and the appreciation of risks in clinical trials.

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3.  A questionnaire on factors influencing children's assent and dissent to non-therapeutic research.

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Review 4.  Diversified harmony: supranational and domestic regulation of pediatric clinical trials in the European Union.

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5.  Conflicts of interest in research on children.

Authors:  M Evans
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6.  Parental consent in paediatric clinical research.

Authors:  H Chappuy; F Doz; S Blanche; J-C Gentet; G Pons; J-M Tréluyer
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7.  Convention for the protection of human rights and dignity of the human being with regard to the application of biology and medicine: convention on human rights and biomedicine (adopted by the Committee of Ministers on 19 November 1996). Council of Europe Convention of Biomedicine.

Authors: 
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8.  Communication of randomization in childhood leukemia trials.

Authors:  Eric Kodish; Michelle Eder; Robert B Noll; Kathleen Ruccione; Beverly Lange; Anne Angiolillo; Rebecca Pentz; Stephen Zyzanski; Laura A Siminoff; Dennis Drotar
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9.  Neonatal research and the validity of informed consent obtained in the perinatal period.

Authors:  Hubert O Ballard; Lori A Shook; Nirmala S Desai; K J S Anand
Journal:  J Perinatol       Date:  2004-07       Impact factor: 2.521

10.  Informed consent in clinical research in France: assessment and factors associated with therapeutic misconception.

Authors:  I S Durand-Zaleski; C Alberti; P Durieux; X Duval; S Gottot; Ph Ravaud; S Gainotti; C Vincent-Genod; D Moreau; P Amiel
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  8 in total

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Journal:  Eur J Pediatr       Date:  2013-01-05       Impact factor: 3.183

2.  Ethical considerations of researchers conducting pediatric clinical drug trials: a qualitative survey in two Belgian university children's hospitals.

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4.  Consent procedures in pediatric biobanks.

Authors:  Noor Aa Giesbertz; Annelien L Bredenoord; Johannes Jm van Delden
Journal:  Eur J Hum Genet       Date:  2014-12-24       Impact factor: 4.246

5.  Pain in Intellectually Disabled Children: Towards Evidence-Based Pharmacotherapy?

Authors:  Abraham J Valkenburg; Tom G de Leeuw; Monique van Dijk; Dick Tibboel
Journal:  Paediatr Drugs       Date:  2015-10       Impact factor: 3.022

6.  Personalized assent for pediatric biobanks.

Authors:  Noor A A Giesbertz; Karen Melham; Jane Kaye; Johannes J M van Delden; Annelien L Bredenoord
Journal:  BMC Med Ethics       Date:  2016-10-12       Impact factor: 2.652

Review 7.  Medical decision-making in children and adolescents: developmental and neuroscientific aspects.

Authors:  Petronella Grootens-Wiegers; Irma M Hein; Jos M van den Broek; Martine C de Vries
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Review 8.  Ethical issues in genomics research on neurodevelopmental disorders: a critical interpretive review.

Authors:  S Mezinska; L Gallagher; M Verbrugge; E M Bunnik
Journal:  Hum Genomics       Date:  2021-03-12       Impact factor: 4.639

  8 in total

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