Staphylococcus aureus bacteraemia treatment outcomes in patients receiving ticagrelor vs a propensity-matched cohort receiving clopidogrel.
Chris A Gentry, Riley J Williams, Charles M Whitman...
https://pubmed.ncbi.nlm.nih.gov/36736927Actively Recruiting
Led by Todd C. Lee MD MPH FIDSA · Updated on 2026-03-20
300
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are evaluating the effects of clopidogrel compared to aspirin in patients with Staphylococcus aureus bloodstream infections who are already taking aspirin for secondary prevention of cardiovascular events. This open-label randomized controlled trial aims to determine if switching from aspirin to clopidogrel, which may have activity against S. aureus, can improve patient outcomes. The study is a sub-study of the larger Staphylococcus aureus Network Adaptive Platform (SNAP) trial and could lead to a future Phase 3 trial for broader populations. Participants will be randomly assigned to either stop aspirin and start clopidogrel without a loading dose or continue their current aspirin treatment. The trial is designed to compare these two approaches for cardiovascular risk reduction in the context of S. aureus infection. The treatment period coincides with enrollment in the SNAP trial, and patients are monitored throughout. During the study, researchers will assess outcomes at 90 days after enrollment in the SNAP trial, focusing on a ranking system called the Desirability of Outcome Ranking (DOOR). Additional measures include clinical failure, adverse events leading to treatment changes, mortality, infectious complications, bleeding events, thromboembolic events, strokes, heart attacks, and other arterial events. Participation involves regular monitoring and data collection as part of the SNAP trial protocol up to the study end date in January 2030.
CONDITIONS
Clopidogrel vs. Aspirin for Cardiovascular Risk Reduction in Patients With S. Aureus Bacteremia
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 90 days post enrollment
Participants will either switch from aspirin to clopidogrel or continue their existing aspirin as part of the study treatment.
Total: 1 location
1
McGill University Health Centre (Royal Victoria Hospital and Montreal General Hospital)
Montreal, Quebec, Canada, H4A3S1
Actively Recruiting
L
Lina Petrella
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Have more questions? Get in touch with our team for quick support
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Chris A Gentry, Riley J Williams, Charles M Whitman...
https://pubmed.ncbi.nlm.nih.gov/36736927Steven Y C Tong, Jocelyn Mora, Asha C Bowen...
https://pubmed.ncbi.nlm.nih.gov/35717634Aisling R Caffrey, Haley J Appaneal, Kerry L LaPlante...
https://pubmed.ncbi.nlm.nih.gov/35416712