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The ethical framework for performing research with rare inherited neurometabolic disease patients.

Viviana GiannuzziHugo DevliegerLucia MargariViveca Lena OdlindLamis RagabCinzia Maria BellettatoFrancesca D'AvanzoChristina LampeLinda CassisElisenda Cortès-SaladelafontÁngels Garcia CazorlaIvo BarićLjerka Cvitanović-ŠojatKsenija FumićChristine I DaliFranco BartoloniFedele BonifaziMaurizio ScarpaAdriana Ceci
Published in: European journal of pediatrics (2017)
Several recommendations and guidelines on ethical aspects are applicable to the inherited neurometabolic disease research in Europe, even though they suffer from the lack of a common ethical approach. What is Known: • When planning and conducting clinical trials, sponsors and researchers know that clinical trials are to be performed according to well-established ethical rules, and patients should be aware about their rights. • In the cases of paediatric patients, vulnerable patients unable to provide consent, genetic diseases' further rules apply. What is New: • This work discusses which ethical rules apply to ensure protection of patient's rights if all the above-mentioned features coexist. • This work shows available data and information on how these rules have been applied.
Keyphrases
  • end stage renal disease
  • clinical trial
  • ejection fraction
  • peritoneal dialysis
  • prognostic factors
  • emergency department
  • gene expression
  • intensive care unit
  • decision making
  • dna methylation
  • study protocol