Grant: Operating Grant: COVID-19 Rapid Research Funding Opportunity - Therapeutics
University of Manitoba
$3,573,336.00
ANTI-THROMBOTIC THERAPY TO AMELIORATE COMPLICATIONS OF COVID-19 (ATTACC): A randomized, international, multi-centre, adaptive, controlled clinical trial
FY 2020-21
Summary
COVID-19 is associated with an unusually high risk of blood clots. Small studies have suggested that anticoagulant (blood thinning) medications that prevent blood clots from forming or travelling may improve the health and survival of hospitalized patients with COVID-19. The goal of this study is to establish whether anticoagulants called heparins can improve outcomes in patients with COVID-19. This study will compare patients who are treated with higher doses of heparin to those that receive usual clinical care, which typically includes low dose heparin. It will measure whether a patient requires intubation (a breathing tube) and need to be on a ventilator, or dies within 30 days of the treatment. It will also monitor patients for other important outcomes such as bleeding, heart attacks, and blood clots.
This trial follows a Bayesian adaptive design. Adaptive designs can make clinical trials more flexible by taking into account early results to modify the course of the trial. This is particularly helpful during the COVID-19 pandemic because the trial will make better use of resources in a short timeframe. The trial also uses a randomization method called response-adaptive randomization which allows more patients to be assigned to the superior treatment as the trial progresses.
The trial will enroll up to 3000 patients in Canada, the US, Brazil, and Mexico. Participants will be randomly assigned to the investigational arm will receive higher dose unfractionated heparin or low-molecular-weight heparin for up to 14 days. Participants assigned to the control arm will receive usual clinical care, which may include low dose unfractionated heparin or low-molecular-weight heparin.
This trial includes collaborations with two large Canadian research networks, the Canadian Venous Thromboembolism Research Network (CanVECTOR) and the Canadian Critical Care Trials Group (CCCTG), and is being conducted in partnership with another global COVID-19 trial called REMAP-CAP.
Department
Program
Operating Grant: COVID-19 Rapid Research Funding Opportunity - Therapeutics
Recipient
Location
Manitoba, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
429655
Name
Zarychanski Ryan
Region
Manitoba
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Clinical
Prcname2
COVID-19 Rapid Research - Therapeutics
Projecttitle
ANTI-THROMBOTIC THERAPY TO AMELIORATE COMPLICATIONS OF COVID-19 (ATTACC): A randomized, international, multi-centre, adaptive, controlled clinical trial
Programtype2
Operating Grants
Orgnameinp2
University of Manitoba
Cihramount2
$3,573,336
Cihrequipment2
$0
Programname2
Operating Grant: COVID-19 Rapid Research Funding Opportunity - Therapeutics
Keyworddelim
Anti-Thrombotic; Bayesian Adaptive; Covid-19; Sepsis; Thrombosis
Abstract
COVID-19 is associated with an unusually high risk of blood clots. Small studies have suggested that anticoagulant (blood thinning) medications that prevent blood clots from forming or travelling may improve the health and survival of hospitalized patients with COVID-19. The goal of this study is to establish whether anticoagulants called heparins can improve outcomes in patients with COVID-19. This study will compare patients who are treated with higher doses of heparin to those that receive usual clinical care, which typically includes low dose heparin. It will measure whether a patient requires intubation (a breathing tube) and need to be on a ventilator, or dies within 30 days of the treatment. It will also monitor patients for other important outcomes such as bleeding, heart attacks, and blood clots.
This trial follows a Bayesian adaptive design. Adaptive designs can make clinical trials more flexible by taking into account early results to modify the course of the trial. This is particularly helpful during the COVID-19 pandemic because the trial will make better use of resources in a short timeframe. The trial also uses a randomization method called response-adaptive randomization which allows more patients to be assigned to the superior treatment as the trial progresses.
The trial will enroll up to 3000 patients in Canada, the US, Brazil, and Mexico. Participants will be randomly assigned to the investigational arm will receive higher dose unfractionated heparin or low-molecular-weight heparin for up to 14 days. Participants assigned to the control arm will receive usual clinical care, which may include low dose unfractionated heparin or low-molecular-weight heparin.
This trial includes collaborations with two large Canadian research networks, the Canadian Venous Thromboembolism Research Network (CanVECTOR) and the Canadian Critical Care Trials Group (CCCTG), and is being conducted in partnership with another global COVID-19 trial called REMAP-CAP.
Competitiondate
202005
Approvedterm2
1 yr 0 mth
Pinamesdelim
Zarychanski, Ryan; Escobedo, Jorge; Goligher, Ewan C; Lawler, Patrick R; Nicolau, Jose C
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $3,573,336~ $0~