When is waiver of consent appropriate in a neonatal clinical trial?

Pediatrics. 2014 Nov;134(5):1006-12. doi: 10.1542/peds.2014-0207. Epub 2014 Oct 6.

Abstract

It is difficult to do scientifically rigorous research on treatments that must be administered urgently or emergently. Therefore, such treatments are often provided without a strong evidence base. Research would be facilitated if it were permissible to waive the requirement for parental consent. However, that raises a different set of concerns. Federal regulations allow waiver of the requirement for consent but only if studies meet certain conditions. Institutional review boards must decide whether those conditions are met. Sometimes, reasonable people disagree. We present and analyze a protocol for which investigators request a waiver of consent.

Keywords: child; consent; equipoise; ethics; meconium aspiration; research.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Emergency Medical Services / ethics*
  • Emergency Medical Services / methods
  • Humans
  • Infant, Newborn*
  • Informed Consent / ethics
  • Parental Consent / ethics*
  • Randomized Controlled Trials as Topic / ethics*
  • Randomized Controlled Trials as Topic / methods