Phase
Condition
Myocardial Ischemia
Atherosclerosis
Hypercholesterolemia
Treatment
Enteric-coated aspirin
Hybrid strategy
Plain aspirin
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Adult patients (≥18 years) with documented ASCVD defined as at least one of thefollowing:
Coronary artery disease (CAD):
- Previous or recent documented type I myocardial infarction *(if notspecified, will be assumed as type I)
- History of coronary revascularization (percutaneous coronary interventionor coronary artery bypass graft surgery)
- History of obstructive CAD (>50% stenosis) documented by coronary computedtomography (CT) or conventional angiography
- Peripheral arterial disease (PAD):
- Previous or recent acute ischemic limb event (>7 days prior)
- History of previous endovascular/surgical lower or upper extremitiesrevascularization for an atherosclerotic cause
- History of ulcer or lower extremities amputation due to ASCVD.
- Carotid arterial diseases:
- History of previous endovascular/surgical carotid artery revascularizationfor atherosclerotic causes
- History of > 50% carotid artery stenosis based on documented imaging tests (Duplex US, CT angiography, magnetic resonance angiography, orconventional angiography)
- Ischemic stroke:
- History of recent or previous documented ischemic stroke not due to atrialfibrillation, endocarditis, or systemic hypoperfusion/hypotension, beingtreated with low-dose aspirin
Inhabitant of Tehran province
Willing to participate and able to provide written informed consent
Exclusion
Exclusion Criteria:
Being within 72 days of acute/unstable atherosclerotic cardiovascular events (acutemyocardial infarction, acute limb event, and acute ischemic stroke), or within 72hours of revascularization.
Patients receiving triple antithrombotic therapy
History of upper gastrointestinal bleeding within the past 30 days
History of intracranial hemorrhage within the past 30 days
End-stage kidney disease with estimated creatinine clearance < 15 mL/min, orundergoing hemodialysis or peritoneal dialysis
Known comorbidities associated with poor prognosis (e.g., metastatic cancer) inconjunction with an estimated life expectancy of less than one year according to thetreating clinician
Any other conditions that make the participants unsuitable for recruitment orfollow-up (e.g., illiteracy)
Not having aspirin as part of the planned durable treatment regimen
Inability to receive/read text messages/phone calls by personal mobile phone (orthat of a caregiver who lives with the patient and is willing to relay messages)
The full list of exclusion criteria is provided in the study protocol
Study Design
Study Description
Connect with a study center
Rajaie Cardiovascular Medical and Research Center
Tehran, 1995614331
Iran, Islamic Republic ofActive - Recruiting
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