作者: T. Engelhardt , D. Ayansina , G. T. Bell , V. Oshan , J. S. Rutherford
DOI: 10.1111/ANAE.14520
关键词: Coordinating Investigator 、 Incidence (epidemiology) 、 Waiver 、 Medicine 、 Observational Trial 、 Family medicine 、 Quality management 、 Paediatric anaesthesia 、 Guardian 、 Inclusion (education)
摘要: APRICOT was registered with ClinicalTrials.gov (NCT01878760). The funding source (ESA) provided the infrastructure for trial. UK national study coordinating investigator (NM), liaised local investigators regarding their ethics submission process and inclusion period, monitored data entry cleaning. A UK-wide waiver individual patient/family consent granted Caldicott guardian approval given management, anonymisation procedures security. Authors NM, TE DA had full access to all in final responsibility decision submit manuscript. ESA principal approved manuscript content before submission.