Anti-Thrombotic Therapy to Ameliorate Complications of COVID-19 (ATTACC): Study design and methodology for an international, adaptive Bayesian randomized controlled trial.


Journal

Clinical trials (London, England)
ISSN: 1740-7753
Titre abrégé: Clin Trials
Pays: England
ID NLM: 101197451

Informations de publication

Date de publication:
10 2020
Historique:
pubmed: 21 8 2020
medline: 21 10 2020
entrez: 21 8 2020
Statut: ppublish

Résumé

Mortality from COVID-19 is high among hospitalized patients and effective therapeutics are lacking. Hypercoagulability, thrombosis and hyperinflammation occur in COVID-19 and may contribute to severe complications. Therapeutic anticoagulation may improve clinical outcomes through anti-thrombotic, anti-inflammatory and anti-viral mechanisms. Our primary objective is to evaluate whether therapeutic-dose anticoagulation with low-molecular-weight heparin or unfractionated heparin prevents mechanical ventilation and/or death in patients hospitalized with COVID-19 compared to usual care. An international, open-label, adaptive randomized controlled trial. Using a Bayesian framework, the trial will declare results as soon as pre-specified posterior probabilities for superiority, futility, or harm are reached. The trial uses response-adaptive randomization to maximize the probability that patients will receive the more beneficial treatment approach, as treatment effect information accumulates within the trial. By leveraging a common data safety monitoring board and pooling data with a second similar international Bayesian adaptive trial (REMAP-COVID anticoagulation domain), treatment efficacy and safety will be evaluated as efficiently as possible. The primary outcome is an ordinal endpoint with three possible outcomes based on the worst status of each patient through day 30: no requirement for invasive mechanical ventilation, invasive mechanical ventilation or death. Using an adaptive trial design, the Anti-Thrombotic Therapy To Ameliorate Complications of COVID-19 trial will establish whether therapeutic anticoagulation can reduce mortality and/or avoid the need for mechanical ventilation in patients hospitalized with COVID-19. Leveraging existing networks to recruit sites will increase enrollment and mitigate enrollment risk in sites with declining COVID-19 cases.

Sections du résumé

BACKGROUND
Mortality from COVID-19 is high among hospitalized patients and effective therapeutics are lacking. Hypercoagulability, thrombosis and hyperinflammation occur in COVID-19 and may contribute to severe complications. Therapeutic anticoagulation may improve clinical outcomes through anti-thrombotic, anti-inflammatory and anti-viral mechanisms. Our primary objective is to evaluate whether therapeutic-dose anticoagulation with low-molecular-weight heparin or unfractionated heparin prevents mechanical ventilation and/or death in patients hospitalized with COVID-19 compared to usual care.
METHODS
An international, open-label, adaptive randomized controlled trial. Using a Bayesian framework, the trial will declare results as soon as pre-specified posterior probabilities for superiority, futility, or harm are reached. The trial uses response-adaptive randomization to maximize the probability that patients will receive the more beneficial treatment approach, as treatment effect information accumulates within the trial. By leveraging a common data safety monitoring board and pooling data with a second similar international Bayesian adaptive trial (REMAP-COVID anticoagulation domain), treatment efficacy and safety will be evaluated as efficiently as possible. The primary outcome is an ordinal endpoint with three possible outcomes based on the worst status of each patient through day 30: no requirement for invasive mechanical ventilation, invasive mechanical ventilation or death.
CONCLUSION
Using an adaptive trial design, the Anti-Thrombotic Therapy To Ameliorate Complications of COVID-19 trial will establish whether therapeutic anticoagulation can reduce mortality and/or avoid the need for mechanical ventilation in patients hospitalized with COVID-19. Leveraging existing networks to recruit sites will increase enrollment and mitigate enrollment risk in sites with declining COVID-19 cases.

Identifiants

pubmed: 32815416
doi: 10.1177/1740774520943846
doi:

Substances chimiques

Anticoagulants 0
Antiviral Agents 0
Heparin 9005-49-6

Banques de données

ClinicalTrials.gov
['NCT04372589']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

491-500

Auteurs

Brett L Houston (BL)

Max Rady Faculty of Health Sciences, Max Rady College of Medicine, Department of Internal Medicine, University of Manitoba, Winnipeg, MB, Canada.

Patrick R Lawler (PR)

Peter Munk Cardiac Centre, University Health Network and University of Toronto, Toronto, ON, Canada.
Toronto General Hospital Research Institute, Toronto, ON, Canada.
Interdepartmental Division of Critical Care Medicine, University of Toronto, Toronto, ON, Canada.

Ewan C Goligher (EC)

Toronto General Hospital Research Institute, Toronto, ON, Canada.
Interdepartmental Division of Critical Care Medicine, University of Toronto, Toronto, ON, Canada.
Department of Medicine, Division of Respirology, University Health Network, Toronto, ON, Canada.

Michael E Farkouh (ME)

Peter Munk Cardiac Centre, University Health Network and University of Toronto, Toronto, ON, Canada.

Charlotte Bradbury (C)

Faculty of Health Sciences, University of Bristol, Bristol, UK.

Marc Carrier (M)

Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.

Vlad Dzavik (V)

Peter Munk Cardiac Centre, University Health Network and University of Toronto, Toronto, ON, Canada.

Dean A Fergusson (DA)

Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.

Robert A Fowler (RA)

Department of Medicine, Sunnybrook Health Sciences Centre and University of Toronto, Toronto, ON, Canada.

Jean-Phillippe Galanaud (JP)

Department of Medicine, Sunnybrook Health Sciences Centre and University of Toronto, Toronto, ON, Canada.

Peter L Gross (PL)

Thrombosis and Atherosclerosis Research Institute, Department of Medicine, McMaster University & Hamilton Health Sciences, Hamilton, ON, Canada.

Emily G McDonald (EG)

Clinical Practice Assessment Unit, Department of Medicine, McGill University Health Centre, Montreal, QC, Canada.

Mansoor Husain (M)

Peter Munk Cardiac Centre, University Health Network and University of Toronto, Toronto, ON, Canada.

Susan R Kahn (SR)

Center for Clinical Epidemiology, Jewish General Hospital/Lady Davis Institute, Division of Internal Medicine, Department of Medicine, McGill University, Montreal, QC, Canada.

Anand Kumar (A)

Max Rady Faculty of Health Sciences, Max Rady College of Medicine, Department of Internal Medicine, University of Manitoba, Winnipeg, MB, Canada.

John Marshall (J)

Department of Surgery, St Michael's Hospital and the University of Toronto, Toronto, ON, Canada.

Srinivas Murthy (S)

The University of British Columbia, Vancouver, BC, Canada.

Arthur S Slutsky (AS)

Keenan Research Centre at the Li Ka Shing Knowledge Institute, St. Michael's Hospital and Departments of Medicine, Surgery, and Biomedical Engineering, University of Toronto, Toronto, ON, Canada.

Alexis F Turgeon (AF)

Department of Anesthesiology and Critical Care Medicine, Division of Critical Care Medicine, Faculty of Medicine, Université Laval, Québec, QC, Canada.
CHU de Québec - Université Laval Research Centre, Population Health and Optimal Health Practices Research Unit, Trauma-Emergency-Critical Care Medicine, Université Laval, Québec, QC, Canada.

Scott M Berry (SM)

Berry Consultants, LLC, Austin, TX, USA.

Robert S Rosenson (RS)

The Zena and Michael A. Wiener Cardiovascular Institute, Marie-Josee and Henry R. Kravis Center for Cardiovascular Health, Mount Sinai Hospital, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Jorge Escobedo (J)

Medical Research Unit on Clinical Epidemiology, Mexican Social Security Institute, Mexico City, Mexico.

Jose C Nicolau (JC)

Instituto do Coracao (InCor), Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, Brazil.

Lindsay Bond (L)

Ozmosis Research Inc., Toronto, ON, Canada.

Bridget-Anne Kirwan (BA)

Department of Clinical Research, SOCAR Research SA, Nyon, Switzerland.
Faculty of Epidemiology and Public Health, London School of Hygiene and Tropical Medicine, London, England.

Sophie de Brouwer (S)

Department of Clinical Research, SOCAR Research SA, Nyon, Switzerland.

Ryan Zarychanski (R)

Max Rady Faculty of Health Sciences, Max Rady College of Medicine, Department of Internal Medicine, University of Manitoba, Winnipeg, MB, Canada.
Research Institute in Oncology and Hematology, CancerCare Manitoba, Winnipeg, MB, Canada.

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