Skip to main content
Archives of Disease in Childhood. Fetal and Neonatal Edition logoLink to Archives of Disease in Childhood. Fetal and Neonatal Edition
. 2003 May;88(3):F166–F167. doi: 10.1136/fn.88.3.F166

Obtaining consent for neonatal research

P Allmark, S Mason, A Gill, C Megone
PMCID: PMC1721554  PMID: 12719385

Full Text

The Full Text of this article is available as a PDF (59.7 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Mason S. A., Allmark P. J. Obtaining informed consent to neonatal randomised controlled trials: interviews with parents and clinicians in the Euricon study. Lancet. 2000 Dec 16;356(9247):2045–2051. doi: 10.1016/s0140-6736(00)03401-2. [DOI] [PubMed] [Google Scholar]
  2. Snowdon C., Garcia J., Elbourne D. Making sense of randomization; responses of parents of critically ill babies to random allocation of treatment in a clinical trial. Soc Sci Med. 1997 Nov;45(9):1337–1355. doi: 10.1016/s0277-9536(97)00063-4. [DOI] [PubMed] [Google Scholar]
  3. UK collaborative randomised trial of neonatal extracorporeal membrane oxygenation. UK Collaborative ECMO Trail Group. Lancet. 1996 Jul 13;348(9020):75–82. [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood Fetal and Neonatal Edition are provided here courtesy of BMJ Publishing Group

RESOURCES