Parental comprehension of the benefits/risks of first-line randomised clinical trials in children with solid tumours: a two-stage cross-sectional interview study

OBJECTIVES: To analyse the parental understanding of informed consent information in first-line randomised clinical trials (RCTs) including children with malignant solid tumours and to assess parents’ needs for decision-making. DESIGN: Observational prospective study. SETTING: 3 paediatric oncology...

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Bibliografische gegevens
Hoofdauteurs: Chappuy, Hélène, Bouazza, Naim, Minard-Colin, Veronique, Patte, Catherine, Brugières, Laurence, Landman-Parker, Judith, Auvrignon, Anne, Davous, Dominique, Pacquement, Hélène, Orbach, Daniel, Tréluyer, Jean Marc, Doz, François
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BMJ Publishing Group 2013
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Ethics
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3657641/
https://ncbi.nlm.nih.gov/pubmed/23793670
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjopen-2013-002733
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