When is it impractical to ask informed consent? A systematic review

SJM Laurijssen, R van der Graaf, WB van Dijk… - Clinical …, 2022 - journals.sagepub.com
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 …

[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 …

A preliminary study of pneumonia etiology among hospitalized children in Kenya

LL Hammitt, S Kazungu, SC Morpeth… - Clinical infectious …, 2012 - academic.oup.com
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 …

Randomised controlled trial of oxygen therapy and high-flow nasal therapy in African children with pneumonia

K Maitland, S Kiguli, P Olupot-Olupot… - Intensive care …, 2021 - Springer
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 …

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 …

How parents and practitioners experience research without prior consent (deferred consent) for emergency research involving children with life threatening conditions …

K Woolfall, L Frith, C Gamble, R Gilbert, Q Mok… - BMJ open, 2015 - bmjopen.bmj.com
Objective Alternatives to prospective informed consent to enable children with life-
threatening conditions to be entered into trials of emergency treatments are needed. Across …

Immediate transfusion in African children with uncomplicated severe anemia

K Maitland, S Kiguli, P Olupot-Olupot… - … England Journal of …, 2019 - Mass Medical Soc
Abstract Background The World Health Organization recommends not performing
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)

S Uyoga, P Olupot-Olupot, R Connon… - The Lancet Child & …, 2022 - thelancet.com
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 …

Guidance on clinical research involving infants, children and young people: an update for researchers and research ethics committees

N Modi, J Vohra, J Preston, C Elliott… - Archives of disease in …, 2014 - adc.bmj.com
Background The British Paediatric Association, the forerunner of the Royal College of
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 …

J Lawton, N Hallowell, C Snowdon, JE Norman… - BMC Medical …, 2017 - Springer
Background Obtaining prospective written consent from women to participate in trials when
they are experiencing an obstetric emergency is challenging. Alternative consent pathways …