Phase
Condition
Cardiac Disease
Thrombosis
Hypercholesterolemia
Treatment
aspirin
Clinical Study ID
Ages > 19 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Men or women ≥19 years
Typical chest pain or objective evidence of myocardial ischemia suitable for PCI
Significant de novo coronary artery lesions suitable for DES implantation
Patients who underwent optimized stent implantation either by IVUS or OCT
Using IVUS
MSA >5.5 mm2, or MSA >90% of the MLA at the distal reference segment
Plaque burden <50% with 5 mm of both stent edge
No edge dissection, thrombus or plaque protrusion/stent area <10%
Using OCT
MSA >4.5 mm2, or MSA >90% of the MLA at the distal reference segment
No significant malapposition
No significant edge dissection, thrombus or plaque protrusion/stent area <10%
- The patient or guardian agrees to the study protocol and the schedule of clinicalfollow-up, and provides informed, written consent, as approved by the appropriateInstitutional Review Board/Ethical Committee of the respective clinical site
Exclusion
Exclusion Criteria:
- Angiographic exclusion criteria: any of the followings 1. Bypass graft lesions 2.Lesions in which impaired delivery of imaging catheters is expected:
Extreme angulation (≥90°) proximal to or within the target lesion.
Excessive tortuosity (≥ two 45° angles) proximal to or within the targetlesion.
Heavy calcification proximal to or within the target lesion.
In-stent restenosis
Hypersensitivity or contraindication to device material and its degradants andcobalt, chromium, nickel, platinum, tungsten, acrylic and fluoro polymers thatcannot be adequately pre-medicated.
Persistent thrombocytopenia (platelet count <80,000/l)
Any history of hemorrhagic stroke or intracranial hemorrhage / TIA or ischemicstroke within the past 6 months
A known intolerance or hypersensitivity to a study drug (aspirin, clopidogrel orticagrelor) or heparin
Patients requiring long-term oral anticoagulants or cilostazol
Any surgery requiring general anesthesia or discontinuation of aspirin and/or an ADPantagonist is planned within 12 months after the procedure.
A diagnosis of cancer (other than superficial squamous or basal cell skin cancer) inthe past 3 years or current treatment for the active cancer.
Any clinically significant abnormality identified at the screening visit, physicalexamination, laboratory tests, or electrocardiogram which, in the judgment of theInvestigator, would preclude safe completion of the study.
History of liver cirrhosis (Child-Pugh B or C) or biliary tract obstruction
Life expectancy < 1 years for any non-cardiac or cardiac causes
Cardiogenic shock at the index admission
Patient's pregnant or breast-feeding
Active bleeding or extreme-risk for major bleeding (e.g. active peptic ulcerdisease, gastrointestinal pathology with a high risk for bleeding, malignancies witha high risk for bleeding)
Unwillingness or inability to comply with the procedures described in this protocol.
Study Design
Study Description
Connect with a study center
Bucheon Sejong Hospital
Bucheon,
Korea, Republic ofActive - Recruiting
Dong-A University Hospital
Busan,
Korea, Republic ofActive - Recruiting
Inje University Busan Paik Hospital
Busan,
Korea, Republic ofSite Not Available
Kosin University Gospel Hospital
Busan,
Korea, Republic ofActive - Recruiting
Gyeongsang National University Changwon Hospital
Changwon,
Korea, Republic ofActive - Recruiting
Kangwon National University Hospital
Chuncheon,
Korea, Republic ofActive - Recruiting
Chungbuk National University Hospital
Chungju,
Korea, Republic ofActive - Recruiting
Chungnam National University Sejong Hospital
Chungnam,
Korea, Republic ofActive - Recruiting
Dankook University Hospital
Chungnam,
Korea, Republic ofActive - Recruiting
Daegu Catholic Univ Medical Center
Daegu,
Korea, Republic ofSite Not Available
Keimyung University Dongsan Medical Center
Daegu,
Korea, Republic ofActive - Recruiting
Kyungpook National University Hospital
Daegu,
Korea, Republic ofSite Not Available
Veterans Hospital
Daegu,
Korea, Republic ofSite Not Available
Gangneung Asan Hospital
Gangneung,
Korea, Republic ofActive - Recruiting
Jeonbuk National University Hospital
Jeonju,
Korea, Republic ofActive - Recruiting
Gyeongsang National University Hospital
Jinju,
Korea, Republic ofActive - Recruiting
Asan Medical Center
Seoul,
Korea, Republic ofActive - Recruiting
Kangbuk Samsung Hospital
Seoul,
Korea, Republic ofActive - Recruiting
Korea University Anam Hospital
Seoul,
Korea, Republic ofActive - Recruiting
The Catholic University of Korea, Eunpyeong St. Mary's Hospital
Seoul,
Korea, Republic ofSite Not Available
Veterans Hospital Service Medical Center
Seoul,
Korea, Republic ofActive - Recruiting
Ajou University Hospital
Suwon,
Korea, Republic ofActive - Recruiting
The Catholic University of Korea, ST. Vincent's Hospital
Suwon,
Korea, Republic ofCompleted
Ulsan University Hospital
Ulsan,
Korea, Republic ofActive - Recruiting
Pusan National University Yangsan Hospital
Yangsan,
Korea, Republic ofSite Not Available
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