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Taking people in CanadaPhase 3

Testing Whether Aspirin Prescriptions Are Feasible in Hidden Heart Artery Disease

Tests whether prescribing aspirin or not in people with early heart artery disease is feasible.

Plain-language title generated from the registry record
Registry title: Aspirin in Subclinical Coronary Artery Disease: A Pilot Randomised Controlled Trial

Key facts

Where
Montreal, Québec, and Trois-Rivières, CanadaSee the 3 sites
Phase
Phase 3

Where in Canada

  • Montreal Heart InstituteMontreal, CanadaTaking people
  • Institut Universitaire de Cardiologie et de Pneumologie de Québec (IUCPQ)Québec, CanadaNot yet recruiting
  • Centre hospitalier affilié universitaire régional (CHAUR)Trois-Rivières, CanadaNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Montreal Heart Institute
Trial code
NCT07524335
Record updated
9 November 2026
Original description
In patients with subclinical coronary artery disease, the ASCAD-P study aims to assess the feasibility of a larger phase 3 pragmatic randomized controlled trial comparing prescription versus no prescription of low-dose aspirin in routine clinical practice.Read full original descriptionShow less

Aspirin in Subclinical Coronary Artery Disease: A Pilot Randomised Controlled Trial

In patients with subclinical coronary artery disease, the ASCAD-P study aims to assess the feasibility of a larger phase 3 pragmatic randomized controlled trial comparing prescription versus no prescription of low-dose aspirin in routine clinical practice.

Inclusion: Documented coronary atherosclerosis, as defined by one of the following criteria:; Coronary artery calcium (CAC) score > 0; Cardiac CT angiography (CCTA) / CoroScan: lesions <70% in the right coronary (RCA), left anterior descending (LAD), and circumflex (Cx) arteries or their branches, and <50% in the left main coronary artery; Coronary angiography: lesions <70% in the right coronary (RCA), left anterior descending (LAD), and circumflex (Cx) arteries or their branches, and <50% in the left main coronary artery; if performed, physiological coronary assessments (FFR, dPR, iFR, etc.) and intracoronary imaging (IVUS or OCT) must be negative for significant disease; Willing and able to provide informed consent and comply with study procedures.

Exclusion: Current prescription or clear indication for aspirin, low-molecular-weight heparin (LMWH), direct oral anticoagulants, or any other antithrombotic medication; History of myocardial infarction (MI), coronary revascularization, stroke, transient ischemic attack (TIA), or peripheral arterial revascularization procedure; History of significant bleeding within the past year; Any condition that, in the investigator's judgment, would make participation unsafe for the patient; Severe illness with limited life expectancy (i.e., <5 years); Clear contraindication to aspirin.

ClinicalTrials.gov NCT07524335