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

Last updated: March 14, 2025
Sponsor: Rajaie Cardiovascular Medical and Research Center
Overall Status: Active - Recruiting

Phase

N/A

Condition

Myocardial Ischemia

Atherosclerosis

Hypercholesterolemia

Treatment

Enteric-coated aspirin

Hybrid strategy

Plain aspirin

Clinical Study ID

NCT06541691
4020310
  • Ages > 18
  • All Genders

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Adult patients (≥18 years) with documented ASCVD defined as at least one of thefollowing:

  • Coronary artery disease (CAD):

  1. Previous or recent documented type I myocardial infarction *(if notspecified, will be assumed as type I)
  2. History of coronary revascularization (percutaneous coronary interventionor coronary artery bypass graft surgery)
  3. History of obstructive CAD (>50% stenosis) documented by coronary computedtomography (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 extremitiesrevascularization 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 revascularizationfor atherosclerotic causes
  2. History of > 50% carotid artery stenosis based on documented imaging tests (Duplex US, CT angiography, magnetic resonance angiography, orconventional angiography)
  • Ischemic stroke:
  1. 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

Total Participants: 3000
Treatment Group(s): 3
Primary Treatment: Enteric-coated aspirin
Phase:
Study Start date:
March 06, 2024
Estimated Completion Date:
March 30, 2027

Study Description

  • Background: Aspirin is a key treatment option of patients with atherosclerotic cardiovascular disease (ASCVD). The enteric coating has emerged as a potential solution to minimize the exposure of the gastric mucosa to the medication. However, change in the medication main site of absorption might negatively impact the pharmacokinetics/pharmacodynamics of aspirin and alter its antithrombotic properties, leading to diminished efficacy of the medication. A sufficiently large randomized controlled trial with a long-term follow-up to compare the effectiveness of enteric-coated versus plain aspirin in reducing adverse cardiovascular events and mitigating the adverse effects of the medication in patients with ASCVD is lacking.

Ambient air pollution is a prominent cause of mortality, being associated with 6.7 million deaths worldwide every year, half of which are attributable to cardiovascular causes. Near the half of these deaths is attributable to cardiovascular causes. Several patient-level interventions have been proposed to counteract with the adverse effects of the air pollution, including alerting patients via text message, staying at home, using face masks, or consuming citrus fruits (as a source of vitamin C) during the days with air pollution. However, the effect of implementing these strategies, individually and especially as a group, in mitigating the adverse effects of the air pollution has not yet been studied in a randomized controlled trial powered for clinical outcomes.

The purpose of the current randomized clinical trial is to compare the efficacy and safety of enteric-coated versus plain low-dose (81 mg) aspirin formulations in a double-blind fashion, and an open-label comparison of a multifaceted intervention including a one-page informational flashcard, cell phone message alerting on days with poor air quality to encourage patients not to spend time outdoors or to wear KN-95 facemasks outdoors in those days, and encouraging patients to consume citrus fruits on highly polluted days (hereafter referred to as hybrid strategy), versus usual care, in a multicenter randomized controlled trial (RCT) with a 2x2 factorial design.

  • Design and Randomization method: Multicenter randomized controlled trial with a 2x2 full factorial design with double-blind randomization with a 1:1 allocation ratio to low-dose enteric-coated vs plain aspirin, and open-label randomization with 1:1 allocation ratio to hybrid strategy to reduce the cardiovascular effects of air pollution vs usual care. Permuted block randomization with block sizes of 8, 12 and 16 chosen randomly via an electronic web-based system will be used for the study. The allocation sequence will be concealed. All outcomes will be adjudicated by a Clinical Events Committee blinded to the assigned treatments.

  • Setting: Teaching hospitals in Tehran province, Iran will be involved.

  • Statistical consideration and sample size calculation: An event-driven approach was considered for the calculation of sample size. Considering a relative hazard reduction of 23% in the first (aspirin formulation) randomization and 25% in the second (air pollution mitigation strategy) randomization, to provide a two-sided alpha of 0.05 and a statistical power of 80%, a total number of 460 primary efficacy outcomes for the first randomization and 380 primary efficacy outcomes for the second randomization would be needed. An event-rate of 18.5% for the incidence of primary efficacy outcome in the control arm of the first randomization, and 19.2% for the incidence of primary efficacy outcome in the control arm of the second randomization was assumed per a median follow-up of 2-year. Ultimately, Considering 4% dropout rate per each randomization, a total number of 2920 and 2732 patients would be needed for the first and second randomizations, respectively.

Connect with a study center

  • Rajaie Cardiovascular Medical and Research Center

    Tehran, 1995614331
    Iran, Islamic Republic of

    Active - Recruiting

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