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- W2064667298 abstract "Requirements for informed consent are based on the revered ethical principle of respect for people. How this principle should be applied in randomised trials when valid consent may not be feasible has been hotly debated. However, there has been little effort to ascertain systematically the views of participants in such trials. Obtaining informed consent to neonatal randomised controlled trials: interviews with parents and clinicians in the Euricon studyCurrent standards of informed consent to neonatal research projects could be improved. Research personnel should receive guidance on legal and ethical constraints governing the process. Oral and written information should be given at the same time. Parents could be made aware that research projects have been examined by research ethics committees. Little support was found for the argument that informed consent should be relinquished for the parents' own good. Further study is needed to identify which elements of the process are valued by parents and clinicians in a process that has some unavoidable limitations. Full-Text PDF" @default.
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- W2064667298 title "Views of neonatologists and parents on consent for clinical trials" @default.
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- W2064667298 doi "https://doi.org/10.1016/s0140-6736(00)03395-x" @default.
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