Ethical considerations in conducting pediatric research.

Handb Exp Pharmacol

U.S. Department of Health and Human Services, Food and Drug Administration, Office of the Commissioner, Office of Pediatric Therapeutics, Silver Spring, MD 2011, USA.

Published: February 2012

AI Article Synopsis

  • The importance of including children in clinical research is emphasized, highlighting both the scientific necessity and ethical implications involved.
  • Key ethical considerations are discussed, focusing on children as vulnerable participants and the need for a careful balance between risks and benefits in research design.
  • The chapter proposes an ethical framework for pediatric research and reviews guidelines and regulations from the USA, Canada, and Europe to ensure ethical compliance and participant protection.

Article Abstract

The critical need for pediatric research on drugs and biological products underscores the responsibility to ensure that children are enrolled in clinical research that is both scientifically necessary and ethically sound. In this chapter, we review key ethical considerations concerning the participation of children in clinical research. We propose a basic ethical framework to guide pediatric research, and suggest how this framework might be operationalized in linking science and ethics. Topics examined include: the status of children as a vulnerable population; the appropriate balance of risk and potential benefit in research; ethical considerations underlying study design, including clinical equipoise, placebo controls, and non-inferiority designs; the use of data monitoring committees; compensation; and parental permission and child assent to participate in research. We incorporate selected national (USA) and international guidelines, as well as regulatory approaches to pediatric studies that have been adopted in the USA, Canada, and Europe.

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Source
http://dx.doi.org/10.1007/978-3-642-20195-0_11DOI Listing

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