Àӻ󿬱¸Áö¿ø (CIDR)
Àӻ󿬱¸Áö¿ø (CIDR)
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Research Activity
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IRIS-FFR A Multicenter, prospective cohort to evaluate the natural history of FFR guided Percutaneous Coronary Intervention 📑ClinicalTrials.gov : NCT01366404 -
IRIS-FFR-TANDEM A Multicenter, prospective cohort to evaluate the effect of FFR guided Percutaneous Coronary Intervention in coronary tandem lesions 📑ClinicalTrials.gov : NCT02797561
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FATE-MAIN Fractional Flow Reserve Versus Angiography for Treatment-Decision and Evaluation of Significant Left MAIN Coronary Artery Disease 📑ClinicalTrials.gov : NCT05829889 -
IRIS-MAIN A GLOBAL, MULTICENTER, PROSPECTIVE, REAL WORLD OBSERVATIONAL STUDY FOR LEFT MAIN DISEASE TREATMENT 📑ClinicalTrials.gov : NCT01341327 -
MAIN COMPARE Ten-Year Outcomes of Stents Versus Coronary-Artery Bypass Grafting for Left Main Coronary Artery Disease 📑ClinicalTrials.gov : NCT02791412 -
PRE-COMBAT I Bypass Surgery Versus Angioplasty Using Sirolimus-Eluting Stent in Patients With Left Main Coronary Artery Disease 📑ClinicalTrials.gov : NCT00422968 -
PRE-COMBAT II Evaluation of Outcomes of EES Implantation for Unprotected Left Main Coronary Artery Stenosis 📑ClinicalTrials.gov : NCT01348022
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OCTIVUS Optical Coherence Tomography versus Intravascular Ultrasound Guided Percutaneous Coronary Intervention 📑ClinicalTrials.gov : NCT03394079 -
IRIS Imaging registry Prognosis of Coronary Stenosis Based on Intracoronary Imaging; A Multicenter, Prospective Observational Study 📑ClinicalTrials.gov : NCT02792075 -
PREVENT Preventive PCI or Medical Therapy Alone for Vulnerable Atherosclerotic Coronary Plaque 📑ClinicalTrials.gov : NCT02316886 -
POST-PCI Pragmatic Trial Comparing Symptom-Oriented Versus Routine Stress Testing in High-Risk Patients Undergoing Percutaneous Coronary Intervention 📑ClinicalTrials.gov : NCT03217877
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IRIS BioFreedom Evaluation of Effectiveness and Safety of BIOFREEDOM¢â FAMILY Stent in Routine Clinical Practice; A Multicenter, Prospective Observational Study 📑ClinicalTrials.gov : NCT03190057 -
IRIS-BIOMATRIX Evaluation of Effectiveness and Safety of BIOMATRIX in Routine Clinical Practice; A multicenter, PROSPECTIVE OBSERVATIONAL STUDY 📑ClinicalTrials.gov : NCT01350778 -
IRIS-Cilotax Evaluation of effectiveness and safety of DXR Stent in Routine Clinical Practice; A multicenter prospective observational cohort study 📑ClinicalTrials.gov : NCT01612819 -
IRIS-DEB Evaluation of Effectiveness and Safety of Drug-Eluting Balloon in Routine Clinical Practice; A Multicenter Prospective Observational Cohort Study 📑ClinicalTrials.gov : NCT02038660 -
IRIS DESyne X2 Evaluation of Effectiveness and Safety of DESyne X2 in Routine Clinical Practice; A Multicenter, Prospective Observational Study 📑ClinicalTrials.gov : NCT03588481 -
IRIS-ELEMENT Evaluation of Effectiveness and Safety of PROMUS ELEMENT Stents in Routine Clinical Practice 📑ClinicalTrials.gov : NCT01350791 -
IRIS-GENOUS STEMI Evaluation of Effectiveness and Safety of the GENOUS STENT in ST-Segment Elevation Myocardial Infarction 📑ClinicalTrials.gov : NCT01348373 -
IRIS-INTEGRITY Evaluation of Effectiveness and Safety of Resolute Integrity DES in Routine Clinical Practice; A Multicenter Prospective Observational Cohort Study 📑ClinicalTrials.gov : NCT01392846 -
IRIS-NOBORI Evaluation of Effectiveness and Safety of NOBORI stent in Routine Clinical Practice; A multicenter, PROSPECTIVE OBSERVATIONAL STUDY 📑ClinicalTrials.gov : NCT01348360 -
IRIS-ONYX Evaluation of Effectiveness and Safety of Resolute Onyx¢â and Onyx Frontier¢â in Routine Clinical Practice; A Multicenter, Prospective Observational Study 📑ClinicalTrials.gov : NCT02593994 -
IRIS-Orsiro Evaluation of Effectiveness and Safety of Orsiro¢â in Routine Clinical Practice; A Multicenter, Prospective Observational Study 📑ClinicalTrials.gov : NCT02039739 -
IRIS Skypoint a Non-randomized, Prospective, Open-label Registry to Compare the Effectiveness and Safety of XIENCE Skypoint¢â Stents Versus Other DESs in Patients With Coronary Artery Disease 📑ClinicalTrials.gov : NCT05981911 -
IRIS-Premier Evaluation of Effectiveness and Safety of Promus PREMIER in Routine Clinical Practice; A Multicenter, Phase-IV, Prospective Observational Study 📑ClinicalTrials.gov : NCT02060968 -
IRIS-PRIME Evaluation of Effectiveness and Safety of XIENCE PRIME¢â in Routine Clinical Practice; A Multicenter, Prospective Observational Study 📑ClinicalTrials.gov : NCT01348399 -
IRIS-ROTA Evaluation of Effectiveness and Safety of Rotational Atherectomy in Routine Clinical Practice; A Multicenter, Prospective Observational Study 📑ClinicalTrials.gov : NCT03427996 -
IRIS Sierra Evaluation of Effectiveness and Safety of XIENCE Sierra in Routine Clinical Practice; A MULTICENTER, PROSPECTIVE OBSERVATIONAL STUDY 📑ClinicalTrials.gov : NCT03967158 -
IRIS-Tansei Evaluation of Effectiveness and Safety of Ultimaster¢â Tansei¢â Stent in Routine Clinical Practice; A Multicenter, Prospective Observational Study 📑ClinicalTrials.gov : NCT04443530 -
IRIS-SYNERGY Evaluation of Effectiveness and Safety of Synergy¢â Stent in Routine Clinical Practice; A Multicenter, Prospective Observational Study 📑ClinicalTrials.gov : NCT02720419 -
IRIS Synergy XD And Megatron Evaluation of Effectiveness and Safety of Synergy¢â XD Stent and Synergy Megatron¢â Stent in Routine Clinical Practice; A Multicenter, Prospective Observational Study 📑ClinicalTrials.gov : NCT05044273 -
IRIS Coroflex ISAR NEO registry Evaluation of Effectiveness and Safety of Coroflex ISAR NEO Stent in Routine Clinical Practice; A Multicenter, Prospective Observational Study 📑ClinicalTrials.gov : NCT06177743 -
IRIS-ULTIMASTER Evaluation of Effectiveness and Safety of Ultimaster¢ç Stent in Routine Clinical Practice; A Multicenter, Prospective Observational Study 📑ClinicalTrials.gov : NCT02719106 -
IRIS-Xpedition/Alpine/Sierra Evaluation of Effectiveness and Safety of XIENCE Xpedition/Alpine/Sierra in Routine Clinical Practice; A MULTICENTER, PROSPECTIVE OBSERVATIONAL STUDY 📑ClinicalTrials.gov : NCT02042300 -
K-XIENCE Evaluation of Effectiveness and Safety of Everolimus-Eluting Stents in Routine Clinical Practice 📑ClinicalTrials.gov : NCT01350869 -
DESSIAN Evaluation of Diabetic Effects on Clinical Outcomes After Sirolimus-Eluting Stents in the AsIAN Population 📑ClinicalTrials.gov : NCT00997711
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DEFINE-DM Diabetes-Centered Evaluation of Revascularization Strategy of Functional and Imaging-CombiNEd State-of-the-Art Percutaneous Coronary Intervention or Coronary-Artery Bypass Grafting in Patients With Diabetes Mellitus and Multivessel Coronary Artery Disease 📑ClinicalTrials.gov : NCT05831085 -
Asan-MV Registry Asan Multivessel Registry 📑ClinicalTrials.gov : NCT02039752 -
BEST Bypass Surgery Versus Everolimus-Eluting Stent Implantation for Multivessel Coronary Artery Disease 📑ClinicalTrials.gov : NCT00997828
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IRIS-CTO Registry Chronic Total Occlusion Registry 📑ClinicalTrials.gov : NCT04041921 -
DECISION-CTO Drug-Eluting Stent Implantation Versus Optimal Medical Treatment in Patients With Chronic Total Occlusion 📑ClinicalTrials.gov : NCT01078051
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ASAN-MI Registry Asan Medical Center Myocardial Infarction Registry 📑ClinicalTrials.gov : NCT03412435
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TAILORED-CHIP TAILored Versus COnventional AntithRombotic StratEgy IntenDed for Complex HIgh-Risk PCI 📑ClinicalTrials.gov : NCT03465644 -
EPIC-CAD Edoxaban Versus Edoxaban With antiPlatelet Agent In Patients With Atrial Fibrillation and Chronic Stable Coronary Artery Disease 📑ClinicalTrials.gov : NCT03718559 -
RENOVATE Long-term Anticoagulation With Oral Factor Xa Inhibitor Versus Vitamin K Antagonist After Mechanical Aortic Valve Replacement 📑ClinicalTrials.gov : NCT04258488 -
PROTECT-HBR Potassium-Competitive Acid Blocker versus pROton-Pump Inhibitor for GastroproTECTion Strategies In Patients at High Gastro-Intestinal Bleeding Risk Receiving Antithrombotic Therapy 📑ClinicalTrials.gov : NCT04416581 -
TICAKOREA Safety and Efficacy of Ticagrelor Versus Clopidogrel in Asian/KOREAn Patients With Acute Coronary Syndromes Intended for Invasive Management 📑ClinicalTrials.gov : NCT02094963 -
OPTIMA Comparison of Low-Dose, Standard-Dose Ticagrelor and Clopidogrel for Inhibition of Platelet Reactivity in Patients With Acute Coronary Syndromes 📑ClinicalTrials.gov : NCT02319941 -
FIMA-DEFER Effect of Fimasartan for Modification of Atheroma Vulnerability in DEFERred Coronary Disease 📑ClinicalTrials.gov : NCT01384747 -
PRIDE Effectiveness of Clopidogrel Resinate in PCI 📑ClinicalTrials.gov : NCT01349777 -
STABLE Statin and Atheroma Vulnerability Evaluation 📑ClinicalTrials.gov : NCT00997880 -
DES-LATE Optimal Duration of Clopidogrel Therapy after Drug-Eluting Stent Implantation to Reduce Late Coronary Arterial Thrombotic Events 📑ClinicalTrials.gov : NCT01186146
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Variant ICD Implantable Cardioverter Defibrillator Versus Optimal Medical Therapy In Patients With Variant Angina Manifesting as Aborted Sudden Cardiac Death 📑ClinicalTrials.gov : NCT02845531
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ENAVO-TAVR ENAVOgliflozin Outcome Trial in Patients With Severe Aortic Stenosis After Transcatheter Aortic Valve Replacement 📑ClinicalTrials.gov : NCT05672836 -
ASAN-AVR Registry ASAN Medical Center Aortic Valve Replacement Registry 📑ClinicalTrials.gov : NCT03298178 -
SENTINEL pilot Registry The Sentinel Registry 📑ClinicalTrials.gov : NCT05217888 -
Asian TAVR Registry The Asian Transcatheter Aortic Valve Replacement Registry 📑ClinicalTrials.gov : NCT02308150 -
ADAPT-TAVR Anticoagulant Versus Dual Antiplatelet Therapy for Preventing Leaflet Thrombosis and Cerebral Embolization After Transcatheter Aortic Valve Replacement 📑ClinicalTrials.gov : NCT03284827
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HOWTO-BRS Anticoagulant Versus Dual Antiplatelet Therapy for Preventing Leaflet Thrombosis and Cerebral Embolization After Transcatheter Aortic Valve Replacement 📑ClinicalTrials.gov : NCT03175523 -
BVS Late Optimal Duration of Antiplatelet Therapy After Bioresorbable Vascular Scaffold Implantation to Reduce Late Coronary Arterial Thrombotic Events 📑ClinicalTrials.gov : NCT02939872 -
IRIS-BVS Evaluation of Effectiveness and Safety of Bioresorbable Vascular Scaffold in Routine Clinical Practice 📑ClinicalTrials.gov : NCT02622100