|

OCT-Guided Stent Optimization for Short-Duration Dual Antiplatelet Therapy in Stable Angina

RECRUITINGN/ASponsored by Korea University Guro Hospital
Actively Recruiting
PhaseN/A
SponsorKorea University Guro Hospital
Started2025-09-30
Est. completion2029-09
Eligibility
Age19 Years+
Healthy vol.Accepted

Summary

This study aims to evaluate whether the use of optical coherence tomography (OCT), an advanced intravascular imaging tool, can improve stent implantation results and make it possible to shorten the duration of dual antiplatelet therapy (DAPT) in patients with stable angina who undergo percutaneous coronary intervention (PCI). PCI with drug-eluting stents is a standard treatment for patients with stable angina, and these patients are usually prescribed DAPT for 6 to 12 months to prevent stent thrombosis and other complications. However, extended use of DAPT increases the risk of bleeding, which can lead to significant medical problems, especially in patients with high bleeding risk. OCT provides detailed, high-resolution images of the coronary arteries and the implanted stents, allowing physicians to optimize stent expansion and positioning. By ensuring that the stent is well-placed and fully expanded, OCT guidance may lower the risk of complications, potentially reducing the need for prolonged DAPT. In this prospective study, patients with stable angina who require stent implantation will be enrolled and treated with OCT-guided PCI followed by a short course of DAPT. Their outcomes will be compared with those managed using conventional strategies. The primary goal of this trial is to determine whether OCT-guided stent optimization can safely support a short-duration DAPT strategy, thereby reducing bleeding risk without compromising protection against ischemic events such as restenosis, myocardial infarction, or stent thrombosis.

Eligibility

Age: 19 Years+Healthy volunteers accepted
Inclusion Criteria:

* Patients who undergo PCI using a cobalt-chromium everolimus-eluting stent (CoCr-EES)
* Diagnosis of stable angina
* Ability and willingness to provide written informed consent approved by the Institutional Review Board (IRB), and to comply with the study protocol and clinical follow-up schedule
* Age ≥ 19 years

Exclusion Criteria:

* Patients diagnosed with acute coronary syndrome (ACS), including unstable angina or acute myocardial infarction
* Contraindications to antiplatelet therapy or OCT imaging
* Presence of lesions with severe stenosis, heavy calcification, or marked vessel tortuosity that prevent passage of a guidewire or catheter
* Patients with previously implanted coronary stents in the target lesion

Conditions3

Coronary Artery DiseaseHeart DiseaseStable Angina

Browse More Trials

Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.