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Starting soon Observational

Drug Coated Balloon vs. Drug-eluting Stent in Patients With Coronary Artery Disease

NCT07442500 · tracked via the Priya Life Science South Korea tracker
Phase
Observational
Started
2026-02-28
Last updated
2026-03-02

Condition(s) studied

Coronary Artery DiseasePercutaneous Coronary Intervention (PCI)

Investigational drug(s) / intervention(s)

Drug coated balloonDrug-eluting stent

Drug coated balloon: Patients receiving drug coated balloon angioplasty for de novo coronary artery disease

Drug-eluting stent: Patients receiving drug-eluting stent implantationfor de novo coronary artery disease

Study summary

Studies exploring the feasibility of drug-eluting balloon (DCB) in de-novo coronary lesions are limited. There are scarce data comparing DCB with drug-eluting stent (DES) in patients with high bleeding risk (HBR), a situation in which long-term maintenance of dual antiplatelet therapy (DAPT) is a clinical dilemma. This target trial emulation aims to compare clinical outcomes between DCB angioplasty and conventional DES implantation in de-novo coronary lesions in patients with coronary artery disease.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients with coronary artery disease undergoing percutaneous coronary intervention * Used devices number less than three (relatively simple lesion) Exclusion Criteria: * Hybrid strategy (DCB and DES use) * Failed percutaneous coronary intervention * Previous revascularization procedure before index percutaneous coronary intervention

Primary outcome measure(s)

  • Rates of MACCE (major adverse cardiac and cerebrovascular events) — 3 years after index procedure
    all-cause death, myocardial infarction, revascularization, and stroke

Trial sites (1)

FacilityCityRegionStatus
Samsung Medical Center Seoul South Korea
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07442500 on ClinicalTrials.gov ↗ ← All trials in South Korea