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Recruiting NCT05320926

NCT05320926 Clopidogrel Versus Aspirin MOnotherapy After 1- to 3-month of Dual-antiplatelet thErapy Following Zotarolimus-eluting Onyx Stents Implantation; C-MODE Trial

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Clinical Trial Summary
NCT ID NCT05320926
Status Recruiting
Phase
Sponsor Yonsei University
Condition Ischemic Heart Disease
Study Type INTERVENTIONAL
Enrollment 3,744 participants
Start Date 2022-07-26
Primary Completion 2028-07-10

Trial Parameters

Condition Ischemic Heart Disease
Sponsor Yonsei University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 3,744
Sex ALL
Min Age 19 Years
Max Age 84 Years
Start Date 2022-07-26
Completion 2028-07-10
Interventions
Clopidogrel monotherapyAspirin monotherapyzotarolimus-eluting stent (Resolute Onyx ®)

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Brief Summary

Previous randomized clinical trials have deomonstrated the efficacy and safety of short-term dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI), however, the single antiplatelet agent to be maintained after short-term DAPT was different. Therefore, which antiplatelet agent to be maintained after short-term DAPT needs further invstigations.

Eligibility Criteria

Inclusion Criteria: 1. Patients ≥19 years 2. Patients who received new generation zotarolimus-eluting Onyx stents implantation for treating ischemic heart disease 3. Provision of informed consent Exclusion Criteria: 1. Age ≥ 85 years 2. Acute myocardial infarction 2\. Left main bifurcation requiring 2-stent technique 3. Pregnant women or women with potential childbearing 4. Life expectancy \< 1 year 5. Inability to follow the patient over the period of 1 year after enrollment, as assessed by the investigator 6. Inability to understand or read the informed consent

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