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When is it impractical to ask informed consent? A systematic review
Background Informed consent is one of the cornerstones of biomedical research with human
subjects. Research ethics committees may allow for a modification or a waiver of consent …
subjects. Research ethics committees may allow for a modification or a waiver of consent …
[PDF][PDF] Institutional review board (IRB) and ethical issues in clinical research
WO Kim - Korean journal of anesthesiology, 2012 - synapse.koreamed.org
Clinical research has expanded tremendously in the past few decades and consequently
there has been growing interest in the ethical guidelines that are being followed for the …
there has been growing interest in the ethical guidelines that are being followed for the …
A preliminary study of pneumonia etiology among hospitalized children in Kenya
Background. Pneumonia is the leading cause of childhood death in the develo** world.
Higher-quality etiological data are required to reduce this mortality burden. Methods. We …
Higher-quality etiological data are required to reduce this mortality burden. Methods. We …
Randomised controlled trial of oxygen therapy and high-flow nasal therapy in African children with pneumonia
Purpose The life-saving role of oxygen therapy in African children with severe pneumonia is
not yet established. Methods The open-label fractional-factorial COAST trial randomised …
not yet established. Methods The open-label fractional-factorial COAST trial randomised …
Restricted fluid bolus volume in early septic shock: results of the Fluids in Shock pilot trial
DP Inwald, R Canter, K Woolfall, P Mouncey… - Archives of disease in …, 2019 - adc.bmj.com
Objective To determine the feasibility of Fluids in Shock, a randomised controlled trial (RCT)
of restricted fluid bolus volume (10 mL/kg) versus recommended practice (20 mL/kg). Design …
of restricted fluid bolus volume (10 mL/kg) versus recommended practice (20 mL/kg). Design …
How parents and practitioners experience research without prior consent (deferred consent) for emergency research involving children with life threatening conditions …
Objective Alternatives to prospective informed consent to enable children with life-
threatening conditions to be entered into trials of emergency treatments are needed. Across …
threatening conditions to be entered into trials of emergency treatments are needed. Across …
Immediate transfusion in African children with uncomplicated severe anemia
Abstract Background The World Health Organization recommends not performing
transfusions in African children hospitalized for uncomplicated severe anemia (hemoglobin …
transfusions in African children hospitalized for uncomplicated severe anemia (hemoglobin …
Sickle cell anaemia and severe Plasmodium falciparum malaria: a secondary analysis of the Transfusion and Treatment of African Children Trial (TRACT)
Background Sickle cell anaemia (SCA) has historically been associated with high levels of
childhood mortality in Africa. Although malaria has a major contribution to this mortality, to …
childhood mortality in Africa. Although malaria has a major contribution to this mortality, to …
Guidance on clinical research involving infants, children and young people: an update for researchers and research ethics committees
Background The British Paediatric Association, the forerunner of the Royal College of
Paediatrics and Child Health (RCPCH), first published guidance in relation to research …
Paediatrics and Child Health (RCPCH), first published guidance in relation to research …
Written versus verbal consent: a qualitative study of stakeholder views of consent procedures used at the time of recruitment into a peripartum trial conducted in an …
Background Obtaining prospective written consent from women to participate in trials when
they are experiencing an obstetric emergency is challenging. Alternative consent pathways …
they are experiencing an obstetric emergency is challenging. Alternative consent pathways …