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Repair of Acute Respiratory Distress Syndrome in COVID-19 by Stromal Cells (REALIST-COVID Trial): A Multicentre, Randomised, Controlled Trial.
Gorman, Ellen A; Rynne, Jennifer; Gardiner, Hannah J; Rostron, Anthony J; Bannard-Smith, Jonathan; Bentley, Andrew M; Brealey, David; Campbell, Christina; Curley, Gerard; Clarke, Mike; Dushianthan, Ahilanadan; Hopkins, Phillip; Jackson, Colette; Kefela, Kallirroi; Krasnodembskaya, Anna; Laffey, John G; McDowell, Cliona; McFarland, Margaret; McFerran, Jamie; McGuigan, Peter; Perkins, Gavin D; Silversides, Jonathan; Smythe, Jon; Thompson, Jacqui; Tunnicliffe, William S; Welters, Ingeborg Dm; Amado-Rodríguez, Laura; Albaiceta, Guillermo; Williams, Barry; Shankar-Hari, Manu; McAuley, Daniel F; O'Kane, Cecilia M.
  • Gorman EA; Queen's University Belfast School of Medicine Dentistry and Biomedical Sciences, 129413, Wellcome Wolfson Institute for Experiemntal Medicine , Belfast, United Kingdom of Great Britain and Northern Ireland.
  • Rynne J; University of Edinburgh MRC Centre for Inflammation Research, 47954, Edinburgh, United Kingdom of Great Britain and Northern Ireland.
  • Gardiner HJ; Queen's University Belfast, 1596, Belfast, United Kingdom of Great Britain and Northern Ireland.
  • Rostron AJ; Newcastle University, Newcastle upon Tyne, United Kingdom of Great Britain and Northern Ireland.
  • Bannard-Smith J; Manchester Royal Infirmary, 105551, Manchester, United Kingdom of Great Britain and Northern Ireland.
  • Bentley AM; University Hospital of South manchester, Respiratory Medicine , Manchester, United Kingdom of Great Britain and Northern Ireland.
  • Brealey D; University of Manchester, 5292, Manchester, United Kingdom of Great Britain and Northern Ireland.
  • Campbell C; University College London, 4919, Bloomsbury Institute of Intensive Care Medicine, London, United Kingdom of Great Britain and Northern Ireland.
  • Curley G; University College London Hospitals NHS Foundation Trust, 8964, Department of Critical Care, London, United Kingdom of Great Britain and Northern Ireland.
  • Clarke M; Northern Ireland Clinical Trials Unit, Belfast, United Kingdom of Great Britain and Northern Ireland.
  • Dushianthan A; Royal College of Surgeons in Ireland, 8863, Anesthesia and Critical Care Medicine, Dublin, Ireland.
  • Hopkins P; Queen's University Belfast Faculty of Medicine Health and Life Sciences, 12209, Centre for Public Health and Medical Research Council All Ireland Hub for Trials Methodology, Belfast, United Kingdom of Great Britain and Northern Ireland.
  • Jackson C; University Hospital Southampton NHS Foundation Trust, 7425, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Kefela K; NIHR Southampton Biomedical Research Centre, 574429, Southampton, United Kingdom of Great Britain and Northern Ireland.
  • Krasnodembskaya A; King's College Hospital, Critical Care, London, United Kingdom of Great Britain and Northern Ireland.
  • Laffey JG; Northern Ireland Clinical Trials Unit, Belfast, United Kingdom of Great Britain and Northern Ireland.
  • McDowell C; Edinburgh Royal Infirmary, Anaesthetics, Critical Care and Pain Medicine, Edinburgh, United Kingdom of Great Britain and Northern Ireland.
  • McFarland M; Queen's University Belfast, Centre for Infection and Immunity, Belfast, United Kingdom of Great Britain and Northern Ireland.
  • McFerran J; National University of Ireland, Galway, Lung Biology Group, Galway, Ireland.
  • McGuigan P; Northern Ireland Clinical Trials Unit, Belfast, United Kingdom of Great Britain and Northern Ireland.
  • Perkins GD; Belfast Health and Social Care Trust, 1602, Belfast, United Kingdom of Great Britain and Northern Ireland.
  • Silversides J; Northern Ireland Clinical Trials Unit, Belfast, United Kingdom of Great Britain and Northern Ireland.
  • Smythe J; Belfast Health and Social Care Trust, 1602, Belfast, United Kingdom of Great Britain and Northern Ireland.
  • Thompson J; Birmingham Heartlands Hospital, Intensive Care Unit, Birmingham, United Kingdom of Great Britain and Northern Ireland.
  • Tunnicliffe WS; Queen's University Belfast School of Medicine Dentistry and Biomedical Sciences, 129413, Wellcome-Wolfson Institute for Experiemntal Medicine , Belfast, United Kingdom of Great Britain and Northern Ireland.
  • Welters ID; NHS Blood and Transplant, 9936, Oxford, United Kingdom of Great Britain and Northern Ireland.
  • Amado-Rodríguez L; NHS Blood and Transplant, 9936, Birmingham, United Kingdom of Great Britain and Northern Ireland.
  • Albaiceta G; University Hospital Birmingham, Edgbaston, Birmingham B15 2TH, United Kingdom, Department of Critical Care, Birmingham, West Midlands, United Kingdom of Great Britain and Northern Ireland.
  • Williams B; Royal Liverpool University Hospital, Critical Care Department, Liverpool, United Kingdom of Great Britain and Northern Ireland.
  • Shankar-Hari M; Hospital Universitario Central de Asturias, 16474, Cardiac Intensive Care Unit, Oviedo, Spain.
  • McAuley DF; Instituto de Investigación Sanitaria del Principado de Asturias, Oviedo, Spain.
  • O'Kane CM; Centro de Investigación Biomédica en Red, 540869, Enfermedades Respiratorias, Madrid, Spain.
Am J Respir Crit Care Med ; 2023 May 08.
Article in English | MEDLINE | ID: covidwho-2314950
ABSTRACT
RATIONALE Mesenchymal stromal cells (MSCs) may modulate inflammation, promoting repair in COVID-19-related Acute Respiratory Distress Syndrome (ARDS).

OBJECTIVES:

We investigated safety and efficacy of ORBCEL-C (CD362-enriched, umbilical cord-derived MSCs) in COVID-related ARDS.

METHODS:

This multicentre, randomised, double-blind, allocation concealed, placebo-controlled trial (NCT03042143) randomised patients with moderate-to-severe COVID-related ARDS to receive ORBCEL-C (400million cells) or placebo (Plasma-Lyte148). MEASUREMENTS The primary safety and efficacy outcomes were incidence of serious adverse events and oxygenation index at day 7 respectively. Secondary outcomes included respiratory compliance, driving pressure, PaO2/FiO2 ratio and SOFA score. Clinical outcomes relating to duration of ventilation, length of intensive care unit and hospital stays, and mortality were collected. Long-term follow up included diagnosis of interstitial lung disease at 1 year, and significant medical events and mortality at 2 years. Transcriptomic analysis was performed on whole blood at day 0, 4 and 7. MAIN

RESULTS:

60 participants were recruited (final analysis n=30 ORBCEL-C, n=29 placebo 1 in placebo group withdrew consent). 6 serious adverse events occurred in the ORBCEL-C and 3 in the placebo group, RR 2.9(0.6-13.2)p=0.25. Day 7 mean[SD] oxygenation index did not differ (ORBCEL-C 98.357.2], placebo 96.667.3). There were no differences in secondary surrogate outcomes, nor mortality at day 28, day 90, 1 or 2 years. There was no difference in prevalence of interstitial lung disease at 1year nor significant medical events up to 2 years. ORBCEL-C modulated the peripheral blood transcriptome.

CONCLUSION:

ORBCEL-C MSCs were safe in moderate-to-severe COVID-related ARDS, but did not improve surrogates of pulmonary organ dysfunction. Clinical trial registration available at www. CLINICALTRIALS gov, ID NCT03042143. This article is open access and distributed under the terms of the Creative Commons Attribution 4.0 International License (https//creativecommons.org/licenses/by/4.0/).
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal subject: Critical Care Year: 2023 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal subject: Critical Care Year: 2023 Document Type: Article