[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100534280":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":8,"centralContacts":13,"locations":18,"responsibleParty":30,"collaborators":7,"id":32,"slug":33,"hasResults":34,"nctId":35,"briefTitle":36,"officialTitle":37,"acronym":7,"eligibilityCriteria":38,"healthyVolunteers":34,"sex":39,"minAge":40,"maxAge":7,"enrollmentInfo":41,"targetDuration":7,"studyType":44,"phases":7,"briefSummary":45,"conditions":46,"keywords":7,"overallStatus":49,"whyStopped":7,"lastUpdateSubmitDate":50,"lastUpdatePostDateStruct":51,"startDateStruct":54,"completionDateStruct":56,"leadSponsor":58,"locationsCount":59},{"fullName":5,"class":6},"Yonsei University","OTHER",null,[9],{"name":10,"affiliation":11,"role":12},"Iksung Cho","Division of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine","PRINCIPAL_INVESTIGATOR",[14],{"name":10,"role":15,"phone":16,"phoneExt":7,"email":17},"CONTACT","82-2-2228-8442","iksungcho@yuhs.ac",[19],{"facility":20,"status":7,"city":21,"state":7,"zip":22,"country":23,"countryCode":7,"cosmosGeoPoint":24,"geoPoint":29,"contacts":7},"Division of Cardiology, Yonsei University Health System, Yonsei University College of Medicine","Seoul","03722","South Korea",{"type":25,"coordinates":26},"Point",[27,28],126.9784,37.566,{"lat":28,"lon":27},{"type":31,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100534280","aware-registry-wearable-ecg-in-structural-heart-interventions-100534280",false,"NCT06236776","AWARE Registry: Wearable ECG in Structural Heart Interventions","Arrhythmia Assessment in Structural Cardiac Interventions Using Wearable ECG Monitoring: AWARE Registry","Inclusion Criteria:\n\n* Adult ≥ 19 year-old\n* Patients who scheduled to perform percutaneous device closure for atrial septal defect or patent foramen ovale\n* Patients provided with the written, informed consent to participate in this study\n\nExclusion Criteria:\n\n* Patients who had paroxysmal, persistent, or chronic AF\n* Life expectancy \\\u003C 12 months\n* Subject who the investigator deems inappropriate to participate in this study","ALL","19 Years",{"count":42,"type":43},150,"ESTIMATED","OBSERVATIONAL","This study is a multi-center (Sinchon Severance hospital \u002F Gangnam Severance hospital), prospective cohort observational study to patients who had undergone structural heart intervention including device closure for secundum type atrial septal defect or Patent foramen ovale. Transthoracic echocardiography will be performed before the procedure, immediately after, and at 6, 18, 30 months after the procedure. Wearable ECG monitoring (\\> 3 days) will be performed before the procedure or immediately after procedure. Demographic, laboratory, hemodynamic data during procedure, and non-invasive imaging dat are obtained.",[47,48],"Atrial Septal Defect","Patent Foramen Ovale","NOT_YET_RECRUITING","2024-01-24",{"date":52,"type":53},"2024-02-01","ACTUAL",{"date":55,"type":43},"2024-02",{"date":57,"type":43},"2028-06",{"name":5,"class":6},1]