Tailored Versus Coventional AntiPlaTelet Strategy Intended After OPTIMIZEd Drug Eluting Stent

Objective: To assess the safety of tailored antiplatelet strategy (short DAPT followed by P2Y12 inhibitor alone) in patients who received optimized DES implantation guided by intravascular imaging (IVUS or OCT)

Design: Prospective, open label, multi-center, dual arm, randomized trial Number of Subjects 3,944 subjects (1972:1972) Study Population: Patients with coronary artery disease undergoing imaging-guided PCI

Study Design:

• Eligible subjects will be randomized 1:1 to a) conventional DAPT strategy or b) tailored anti-platelet strategy (short DAPT followed by P2Y12 inhibitor alone) after optimized DES implantation guided by intravascular imaging.
• All subjects will be clinically followed at 1(or 3), 6, and 12, 18, 24, 36, 48, 50 months

Co-primary Endpoints:

• Clinically relevant bleeding (BARC 2, 3, or 5) at 12 months post-PCI
• Ischemic composite adverse events of all-cause death, MI, ischemia-driven TVR, stent thrombosis at 12 months post-PCI
• Net clinical outcome (NACE) of all-cause death, MI, ischemia-driven TVR, stent thrombosis, BARC 2,3,5 bleeding at 12 months post-PCI

Statistics and Analysis: The study was designed to test the hypothesis that tailored antithrombotic strategy, as compared to the conventional DAPT, would be superior for clinically relevant bleeding, noninferior to the ischemic composite adverse events and NACE. The primary analysis would be evaluated by intention-to-treat analysis. With 3756 (each 1,878) patients, this study has >80% power to detect noninferiority of tailored antiplatelet strategy for ischemic composite adverse event, >85% power to detect noninferiority of tailored antiplatelet strategy for NACE, and >85% power to detect superiority of the tailored antiplatelet arm on clinically relevant bleeding. To compensate for 5% attrition rate, 3,944 (each 1,972) patients will be randomized.

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 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

• 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 target lesion.
• Heavy calcification proximal to or within the target lesion.
• In-stent restenosis
• Hypersensitivity or contraindication to device material and its degradants and cobalt, chromium, nickel, platinum, tungsten, acrylic and fluoro polymers that cannot be adequately pre-medicated.
• Persistent thrombocytopenia (platelet count <80,000/l)
• Any history of hemorrhagic stroke or intracranial hemorrhage / TIA or ischemic stroke within the past 6 months
• A known intolerance or hypersensitivity to a study drug (aspirin, clopidogrel or ticagrelor) or heparin
• Patients requiring long-term oral anticoagulants or cilostazol
• Any surgery requiring general anesthesia or discontinuation of aspirin and/or an ADP antagonist is planned within 12 months after the procedure.
• A diagnosis of cancer (other than superficial squamous or basal cell skin cancer) in the past 3 years or current treatment for the active cancer.
• 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.
• 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 ulcer disease, gastrointestinal pathology with a high risk for bleeding, malignancies with a high risk for bleeding)
• Unwillingness or inability to comply with the procedures described in this protocol.