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RECRUITINGINTERVENTIONAL

Coated or Chewable Aspirin and a Hybrid Strategy to Mitigate Adverse Effects of Air Pollution in Stable Atherosclerotic Disease

Coated or Chewable Aspirin in Patients with Established Atherosclerotic Disease and a Hybrid Strategy to Mitigate the Adverse Effects of Air Pollution: the COATED-AIR Randomized Clinical Trial

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Although both enteric-coated and plain formulations of aspirin are being used commonly, there are no high-quality comparisons between these formulations with respect to clinical efficacy outcomes in patients with atherosclerotic cardiovascular diseases (ASCVD). Air pollution is also a major contributor to the excess risk of cardiovascular events in many regions of the world. However, little is known about the effect of individual-level mitigation strategies against air pollution in reducing cardiovascular outcomes. The purpose of the first randomization is to compare the efficacy and safety of enteric-coated versus plain low-dose (81 mg) aspirin formulations in a double-blind fashion. The second randomization compares a multifaceted intervention including one-page educational flashcard, cell phone text messages alerting participants on polluted days, recommending them to stay indoors or wear KN-95 facemasks provided by the study team in case of necessary outdoor activity, and recommendation to consume citrus fruits on polluted days versus usual care. Both randomization are powered for clinical outcomes and the results will inform practice.

Who May Be Eligible (Plain English)

Who May Qualify: - Adult patients (≥18 years) with documented ASCVD defined as at least one of the following: - Coronary artery disease (CAD): 1. Previous or recent documented type I myocardial infarction \*(if not specified, will be assumed as type I) 2. History of coronary revascularization (percutaneous coronary intervention or coronary artery bypass graft surgery) 3. History of obstructive CAD (\>50% stenosis) documented by coronary computed tomography (CT) or conventional angiography - Peripheral arterial disease (PAD): 1. Previous or recent acute ischemic limb event (\>7 days prior) 2. History of previous endovascular/surgical lower or upper extremities revascularization for an atherosclerotic cause 3. History of ulcer or lower extremities amputation due to ASCVD. - Carotid arterial diseases: 1. History of previous endovascular/surgical carotid artery revascularization for atherosclerotic causes 2. History of \> 50% carotid artery stenosis based on documented imaging tests (Duplex US, CT angiography, magnetic resonance angiography, or conventional angiography) - Ischemic stroke: 1. History of recent or previous documented ischemic stroke not due to atrial fibrillation, endocarditis, or systemic hypoperfusion/hypotension, being treated with low-dose aspirin - Inhabitant of Tehran province - Willing to participate and able to provide written willing to sign a consent form Who Should NOT Join This Trial: - Being within 72 days of acute/unstable atherosclerotic cardiovascular events (acute myocardial infarction, acute limb event, and acute ischemic stroke), or within 72 hours 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, or undergoing hemodialysis or peritoneal dialysis ...See full criteria on ClinicalTrials.gov Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Adult patients (≥18 years) with documented ASCVD defined as at least one of the following: * Coronary artery disease (CAD): 1. Previous or recent documented type I myocardial infarction \*(if not specified, will be assumed as type I) 2. History of coronary revascularization (percutaneous coronary intervention or coronary artery bypass graft surgery) 3. History of obstructive CAD (\>50% stenosis) documented by coronary computed tomography (CT) or conventional angiography * Peripheral arterial disease (PAD): 1. Previous or recent acute ischemic limb event (\>7 days prior) 2. History of previous endovascular/surgical lower or upper extremities revascularization for an atherosclerotic cause 3. History of ulcer or lower extremities amputation due to ASCVD. * Carotid arterial diseases: 1. History of previous endovascular/surgical carotid artery revascularization for atherosclerotic causes 2. History of \> 50% carotid artery stenosis based on documented imaging tests (Duplex US, CT angiography, magnetic resonance angiography, or conventional angiography) * Ischemic stroke: 1. History of recent or previous documented ischemic stroke not due to atrial fibrillation, endocarditis, or systemic hypoperfusion/hypotension, being treated with low-dose aspirin * Inhabitant of Tehran province * Willing to participate and able to provide written informed consent Exclusion Criteria: * Being within 72 days of acute/unstable atherosclerotic cardiovascular events (acute myocardial infarction, acute limb event, and acute ischemic stroke), or within 72 hours 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, or undergoing hemodialysis or peritoneal dialysis * Known comorbidities associated with poor prognosis (e.g., metastatic cancer) in conjunction with an estimated life expectancy of less than one year according to the treating clinician * Any other conditions that make the participants unsuitable for recruitment or follow-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 (or that 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

Treatments Being Tested

DRUG

Enteric-coated aspirin

Enteric-coated aspirin tablet 81 mg, once daily

DRUG

Plain aspirin

Plain aspirin tablet 81 mg, once daily

OTHER

Hybrid strategy

A hybrid strategy composed from: * A one-page educational flashcard * Alerting patients on highly polluted days via text message * Encouraging patients to stay at home or minimizing outdoor activity on highly polluted days * Encouraging patients via text message to wear KN-95 facemasks (provided by the investigators of this study) during outdoors time on highly polluted days * Encouraging patients to consume citrus fruits during highly polluted days

Locations (1)

Rajaie Cardiovascular Medical and Research Center
Tehran, Tehran Province, Iran