Fifteen-minute consultation: An evidence-based approach to research without prior consent (deferred consent) in neonatal and paediatric critical care trials

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Abstract

In the article, the author discusses issues regarding research without consent also called 'deffered consent' in case of pediatric critical care trials. Topics discussed include Exception from Informed Consent (EFIC) by the U.S. Food and Drug Administration (FDA) for the same, conditions for conducting deferred consent research such as urgent requirement of treatment and approval from ethics committee, and points to tell to child's parent such as reason and purpose of the research.

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APA

Woolfall, K., Frith, L., Dawson, A., Gamble, C., & Lyttle, M. D. (2016). Fifteen-minute consultation: An evidence-based approach to research without prior consent (deferred consent) in neonatal and paediatric critical care trials. Archives of Disease in Childhood: Education and Practice Edition, 101(1), 49–53. https://doi.org/10.1136/archdischild-2015-309245

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