Condition: Platelet Aggregation · Type 2 Diabetes · Aspirin · Sponsor: Montreal Heart Institute
This phase 2 study will include patients suffering from type 2 diabetes mellitus and will first study their response to enteric coated aspirin at a dose of 80 mg per day for a 7-day period. Participants with an incomplete platelet inhibition after exposure to EC aspirin at doses of 80 mg once daily will be randomized to a random order of 3 different ASA regimens: EC ASA 162 mg once daily, EC ASA 81 mg twice daily and chewable ASA 40 mg twice daily. The aims are to determine the feasibility of a larger scale trial, and to determine the regimen associated with the lowest proportion of non-responders after randomization. Platelet function will be assessed at baseline and at day 7 of each arms of the study.
This description comes directly from the study's public registry record.
Guillaume Marquis Gravel, MD, MSc · 514-376-3330 · guillaume.marquis.gravel@umontreal.ca
Marie Lordkipanidzé B. Pharm, Ph.D. · 514-376-3330 · marie.lordkipanidze@umontreal.ca
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| Montreal Heart Institute | Montreal, Quebec, Canada | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05702463