Clopidogrel vs. Aspirin for Cardiovascular Risk Reduction in Patients With S. Aureus Bacteremia

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorTodd C. Lee MD MPH FIDSA

About this trial

This is an open-label randomized controlled trial which will enroll patients with S. aureus bacteremia who are already taking aspirin for secondary prevention of cardiovascular events. We will randomize patients to continue their aspirin or change clopidogrel which is also approved for secondary prevention.

Unlike aspirin, clopidogrel may have activity against S. aureus. We wish to determine if changing to clopidogrel 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 Phase 3 RCT in people who do not currently have an indication for clopidogrel.

Eligibility criteria

Qualifiers

None

Disqualifiers

Patient is taking aspirin for secondary prevention of cardiovascular disease (coronary, cerebrovascular, or peripheral vascular disease)

Active bleeding (allowing up to 3 days from platform entry to randomize in the event anti-thrombotic therapy is resumed)

Anticipated major cardiac surgery, neurosurgery, or spine surgery within the next 3 days

Pregnancy

Trial design

Treatments tested in this trial

  • Clopidogrel
  • Aspirin

Treatment groups

300 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Todd C. Lee MD MPH FIDSA

Lead sponsor

McGill University Health Centre/Research Institute of the McGill University Health Centre

Sponsor institution