Optical Coherence Tomography Versus Intravascular Ultrasound Guided Percutaneous Coronary Interventio

Not Applicable

Active, not recruiting

Conditions: Diseases of the circulatory system

Registration Number: KCT0002954

Lead Sponsor: Asan Medical Center

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Active, not recruiting

Sex: All

Target Recruitment: 2000

Inclusion Criteria

Men or women at least 19 years of age
Subjects with coronary artery disease undergoing PCI
The patient or guardian agrees to the study protocol and the schedule of clinical follow-up, and provides informed, written consent, as approved by the appropriate Institutional Review Board/Ethical Committee of the respective clinical site.

Exclusion Criteria

ST-elevation myocardial infarction
Cardiogenic shock or decompensated heart failure with severe LV dysfunction (LVEF) < 30%
Any clinically significant abnormality identified at the screening visit, physical examination, laboratory tests, or electrocardiogram which, in the judgment of the Investigator, would preclude safe completion of the study.
Life expectancy < 1 years for any non-cardiac or cardiac causes
Unwillingness or inability to comply with the procedures described in this protocol.

Study & Design

Study Type: Interventional Study

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Target vessel failure

Secondary Outcome Measures

Name	Time	Method
Device success;Myocardial infarction;Stent thrombosis;Stroke;Any revascularization;Target lesion revascularization;Target vessel revascularization;Repeat hospitalization;Acute kidney injury;Target lesion failure;A composite event of all-cause death and spontaneous MI;A composite of cardiac death and spontaneous MI;A composite of all-cause death, any MI, any repeat revascularization;A composite of cardiac death, target vessel MI, stroke, or clinically significant bleeding