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Study identifier: NCT06650501 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Dabigatran vs. Oral Anti-Xa Inhibitors in S. Aureus Bacteremia

Condition: Staphylococcus Aureus Endocarditis · Staphylococcus Aureus Septicemia · Staphylococcus Aureus Bacteremia  ·  Sponsor: McGill University Health Centre/Research Institute of the McGill University Health Centre

PhasePhase 4
Planned participants300
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is an open-label randomized controlled trial which will enroll patients with S. aureus bacteremia who are already taking oral anticoagulant medications (apixaban, edoxaban, or rivaroxaban) for an approved indication (stroke prevention in atrial fibrillation, prevention or treatment of venous thromboembolism). We will randomize patients to continue their existing medication or change to another medication (dabigatran) which is approved for the original indication. Dabigatran is approved in many countries for the treatment or prevention of venous thromboembolism or preventing stroke in atrial fibrillation. Unlike the other medications listed above, dabigatran seems to have activity against S. aureus in the test tube, in animal models, and in a smaller randomized controlled trial. We wish to determine if changing to dabigatran will improve outcomes in S. aureus bacteremia in people who otherwise would have a reason to be taking it. This study is an approved sub-study of The Staphylococcus aureus Network Adaptive Platform (SNAP) trial (NCT05137119). If positive, this study will support a second RCT in people who do not currently have an indication for anticoagulation.

This description comes directly from the study's public registry record.

Talk to the study team

Lina Petrella  ·  514-934-1934  ·  lina.petrella@muhc.mcgill.ca

Always discuss trial participation with your own doctor first.

Locations (1)

McGill University Health Centre (Royal Victoria Hospital and Montreal General Hospital)Montreal, Quebec, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT06650501