Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33662
Title: Designing acute kidney injury clinical trials.
Austin Authors: Zarbock, Alexander;Forni, Lui G;Ostermann, Marlies;Ronco, Claudio;Bagshaw, Sean M;Mehta, Ravindra L;Bellomo, Rinaldo ;Kellum, John A
Affiliation: Department of Anaesthesiology, Intensive Care and Pain Medicine, University Hospital of Münster, Münster, Germany.;Outcomes Research Consortium, Cleveland, OH, USA.
Department of Critical Care, Royal Surrey Hospital Foundation Trust, Guildford, UK.;School of Medicine, Faculty of Health Sciences, University of Surrey, Guildford, UK.
Department of Intensive Care, King's College London, Guy's & St Thomas' Hospital, London, UK.
Department of Medicine, University of Padova, Padua, Italy.;International Renal Research Institute of Vicenza, Vicenza, Italy.;Department of Nephrology, San Bortolo Hospital, Vicenza, Italy.
Department of Critical Care Medicine, Faculty of Medicine and Dentistry, University of Alberta and Alberta Health Services, Edmonton, Alberta, Canada.
Department of Medicine, University of California San Diego, La Jolla, CA, USA.
Department of Critical Care, University of Melbourne, Parkville, Victoria, Australia.
The Center for Critical Care Nephrology, Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Intensive Care
Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Victoria, Australia.
Department of Intensive Care, Royal Melbourne Hospital, Melbourne, Victoria, Australia.
Issue Date: 2024
Date: 2023
Publication information: Nature Reviews. Nephrology 2024-02; 20(2)
Abstract: Acute kidney injury (AKI) is a common clinical condition with various causes and is associated with increased mortality. Despite advances in supportive care, AKI increases not only the risk of premature death compared with the general population but also the risk of developing chronic kidney disease and progressing towards kidney failure. Currently, no specific therapy exists for preventing or treating AKI other than mitigating further injury and supportive care. To address this unmet need, novel therapeutic interventions targeting the underlying pathophysiology must be developed. New and well-designed clinical trials with appropriate end points must be subsequently designed and implemented to test the efficacy of such new interventions. Herein, we discuss predictive and prognostic enrichment strategies for patient selection, as well as primary and secondary end points that can be used in different clinical trial designs (specifically, prevention and treatment trials) to evaluate novel interventions and improve the outcomes of patients at a high risk of AKI or with established AKI.
URI: https://ahro.austin.org.au/austinjspui/handle/1/33662
DOI: 10.1038/s41581-023-00758-1
ORCID: 0000-0002-2124-1714
0000-0002-0617-5309
0000-0001-9500-9080
0000-0002-6697-4065
0000-0002-0908-2968
0000-0002-1650-8939
0000-0003-1995-2653
Journal: Nature Reviews. Nephrology
PubMed URL: 37653237
ISSN: 1759-507X
Type: Journal Article
Appears in Collections:Journal articles

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