When ethics constrains clinical research: trial design of control arms in "greater than minimal risk" pediatric trials. Academic Article uri icon

Overview

MeSH

  • Animals
  • Biomedical Research
  • Central Nervous System
  • Child
  • Humans
  • Neuronal Ceroid-Lipofuscinoses
  • Pediatrics
  • Research Design
  • Transduction, Genetic

MeSH Major

  • Controlled Clinical Trials as Topic
  • Genetic Therapy
  • Research Subjects

abstract

  • For more than three decades clinical research in the United States has been explicitly guided by the idea that ethical considerations must be central to research design and practice. In spite of the centrality of this idea, attempting to balance the sometimes conflicting values of advancing scientific knowledge and protecting human subjects continues to pose challenges. Possible conflicts between the standards of scientific research and those of ethics are particularly salient in relation to trial design. Specifically, the choice of a control arm is an aspect of trial design in which ethical and scientific issues are deeply entwined. Although ethical quandaries related to the choice of control arms may arise when conducting any type of clinical trials, they are conspicuous in early phase gene transfer trials that involve highly novel approaches and surgical procedures and have children as the research subjects. Because of children's and their parents' vulnerabilities, in trials that investigate therapies for fatal, rare diseases affecting minors, the scientific and ethical concerns related to choosing appropriate controls are particularly significant. In this paper we use direct gene transfer to the central nervous system to treat late infantile neuronal ceroid lipofuscinosis to illustrate some of these ethical issues and explore possible solutions to real and apparent conflicts between scientific and ethical considerations.

publication date

  • September 2011

has subject area

  • Animals
  • Biomedical Research
  • Central Nervous System
  • Child
  • Controlled Clinical Trials as Topic
  • Genetic Therapy
  • Humans
  • Neuronal Ceroid-Lipofuscinoses
  • Pediatrics
  • Research Design
  • Research Subjects
  • Transduction, Genetic

Research

keywords

  • Journal Article

Identity

Language

  • eng

PubMed Central ID

  • PMC3177948

Digital Object Identifier (DOI)

  • 10.1089/hum.2010.230

PubMed ID

  • 21446781

Additional Document Info

start page

  • 1121

end page

  • 1127

volume

  • 22

number

  • 9