[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100431545":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":29,"locations":39,"responsibleParty":53,"collaborators":26,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":63,"eligibilityCriteria":64,"healthyVolunteers":59,"sex":65,"minAge":66,"maxAge":26,"enrollmentInfo":67,"targetDuration":26,"studyType":70,"phases":71,"briefSummary":73,"conditions":74,"keywords":77,"overallStatus":41,"whyStopped":26,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":90},{"fullName":5,"class":6},"Samsung Medical Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"SGLT-2 inhibitor","EXPERIMENTAL","The SGLT-2 inhibitor group will receive SGLT-2 inhibitor once daily until the end of the study period.",[13],"Drug: SGLT2 inhibitor",{"label":15,"type":16,"description":17,"interventionNames":18},"Control","PLACEBO_COMPARATOR","The control group will not receive any additional drugs.",[19],"Other: Control",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DRUG","SGLT2 inhibitor","In patients with AMI and high risk of heart failure, 1:1 randomization will be performed to either SGLT2 inhibitor or control group.",[9],null,{"type":6,"name":15,"description":24,"armGroupLabels":28,"otherNames":26},[15],[30,35],{"name":31,"role":32,"phone":33,"phoneExt":26,"email":34},"Young Bin Song, MD, PhD","CONTACT","82-2-3410-1246","youngbin.song@gmail.com",{"name":36,"role":32,"phone":37,"phoneExt":26,"email":38},"Ki Hong Choi, MD","82-2-3410-6653","cardiokh@gmail.com",[40],{"facility":5,"status":41,"city":42,"state":26,"zip":26,"country":43,"countryCode":26,"cosmosGeoPoint":44,"geoPoint":49,"contacts":50},"RECRUITING","Seoul","South Korea",{"type":45,"coordinates":46},"Point",[47,48],126.9784,37.566,{"lat":48,"lon":47},[51],{"name":36,"role":32,"phone":52,"phoneExt":26,"email":38},"82-2-3410-3419",{"type":54,"investigatorFullName":55,"investigatorTitle":56,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Young Bin Song","Professor","100431545","phase-4-peri-treatment-of-sglt-2-inhibitor-on-myocardial-infarct-size-and-remodeling-index-in-patients-with-acute-myocardial-infarction-and-high-risk-of-heart-failure-undergoing-percutaneous-coronary-intervention-100431545",false,"NCT04899479","Peri-treatment of SGLT-2 Inhibitor on Myocardial Infarct Size and Remodeling Index in Patients With Acute Myocardial Infarction and High Risk of Heart Failure Undergoing Percutaneous Coronary Intervention","Peri-tREatment of SGLT-2 Inhibitor on Myocardial Infarct Size and Remodeling Index Measured by Cardiac maGnetic rEsonance Imaging in Patients With Acute Myocardial Infarction and High Risk of Heart Failure Undergoing Percutaneous Coronary Intervention","PRESTIGE-AMI","Inclusion Criteria:\n\n* 1\\) Subject must be at least 18 years of age 2) Subject is able to verbally confirm understandings of risks, benefits and treatment alternatives of receiving SGLT-2 inhibitor and he\u002Fshe or his\u002Fher legally authorized representative provides written informed consent prior to any study related procedure 3) Diagnosis of Type 1 myocardial infarction (MI) (ST-segment elevation MI \\[STEMI\\] or Non-ST-segment elevation MI \\[NSTEMI\\]) i) Detection of a rise and\u002For fall of cardiac troponin values with at least 1 value above the 99th percentile upper reference limit ii) Symptoms or electrocardiographic changes suggesting myocardial ischemia 4) High risk of heart failure (at least one of the two criteria below are met) i) Left ventricular ejection fraction \\\u003C 50% ii) Symptoms or signs of pulmonary congestion requiring treatment\n\nExclusion Criteria:\n\n* 1\\) Target lesion is not suitable for PCI by operator's decision 2) Patients requiring cardiopulmonary resuscitation due to cardiac arrest before randomization 3) Rescue PCI after thrombolysis or facilitated PCI 4) Previous MI 5) Previous history of heart failure 6) Patients who have been taking SGLT-2 inhibitor 7) Patients with glomerular filtration rate \\\u003C 30ml\u002Fmin\u002F1.73m2 or on dialysis 8) Type 1 diabetes mellitus (DM) 9) Known hypersensitivity or contraindications to study medications (SGLT-2 inhibitor) 10) Pregnant or lactating women 11) Non-cardiac co-morbid conditions are present with life expectancy \\\u003C1 year or that may result in protocol non-compliance (per site investigator's medical judgment)","ALL","18 Years",{"count":68,"type":69},200,"ESTIMATED","INTERVENTIONAL",[72],"PHASE4","We aimed to identify whether SGLT-2 inhibitor administration before and after coronary intervention is effective in reducing the size of infarction and myocardial remodeling in patients with acute myocardial infarction (AMI) and high risk of heart failure, and its mechanism. For this reason, we compared cardiac magnetic resonance imaging (CMR) parameters and clinical outcomes between the SGLT-2 inhibitor group and the control group to confirm the efficacy and safety of SGLT-2 inhibitors.",[75,76],"Acute Myocardial Infarction","Heart Failure",[78,79,80],"Percutaneous Coronary Intervention","Infarct size","Cardiac Magnetic Resonance Imaging","2025-06-22",{"date":83,"type":84},"2025-06-26","ACTUAL",{"date":86,"type":84},"2021-07-05",{"date":88,"type":69},"2025-12-30",{"name":5,"class":6},1]