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Erschienen in: Medicine, Health Care and Philosophy 4/2008

01.12.2008 | Scientific Contribution

Regulating trust in pediatric clinical trials

verfasst von: Wim Pinxten, Herman Nys, Kris Dierickx

Erschienen in: Medicine, Health Care and Philosophy | Ausgabe 4/2008

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Abstract

The participation of minors in clinical trials is essential to provide safe and effective medical care to children. Because few drugs have been tested in children, pediatricians are forced to prescribe medications off-label with uncertain efficacy and safety. In this article, we analyze how the enrollment of minors in clinical trials is negotiated within relationships of mutual trust between clinicians, minors, and their parents. After a brief description of the problems associated with involving minors in clinical research, we consider how existing “relationships of trust” can be used as a place where the concerns of research subjects can be more fully discussed and addressed. Building on the tacit recognition of trust found in The European Clinical Trials Directive we make policy recommendations that allow for clearer, more ethically informed guidelines for enrolling minors in clinical research.
Fußnoten
1
It is estimated that between 7 and 60% of prescriptions in pediatric hospital wards are off-label (Pandoflini and Bonati 2005).
 
2
To correct the commercial disinterest in pediatric drug development, incentives stimulating the pharmaceutical industry to conduct pediatric trials were adopted in US and EU legislation (Rodriguez et al. 2003; FDA Modernization Act of 1997; EC Regulation 1901/2006).
 
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Metadaten
Titel
Regulating trust in pediatric clinical trials
verfasst von
Wim Pinxten
Herman Nys
Kris Dierickx
Publikationsdatum
01.12.2008
Verlag
Springer Netherlands
Erschienen in
Medicine, Health Care and Philosophy / Ausgabe 4/2008
Print ISSN: 1386-7423
Elektronische ISSN: 1572-8633
DOI
https://doi.org/10.1007/s11019-008-9157-8

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