[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"defibrillators\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:defibrillators":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,41,71],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100642822","increasing-law-enforcement-application-of-automated-external-defibrillators-aeds-for-cardiac-arrest-100642822",false,"NCT07649616","Increasing Law Enforcement Application of Automated External Defibrillators (AED)s for Cardiac Arrest","Increasing Law Enforcement Application of Automated External Defibrillators for Cardiac Arrest","Inclusion Criteria:\n\n* Law enforcement officers from agencies in the greater Portland area served by the Portland Cardiac Arrest Epidemiologic Registry\n* aged 18 years of age and older\n\nExclusion Criteria:\n\n* none","ALL","18 Years",{"count":19,"type":20},30,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this study is to learn if an automated external defibrillator (AED) training adjunct video can improve law enforcement self-efficacy, the likelihood of AED application overall, and decrease disparities in women.\n\nParticipants will be asked to:\n\n* complete a brief initial survey\n* view an AED training adjunct video\n* complete another survey following the video",[26,27],"Heart Arrest, Out-Of-Hospital","Defibrillators","NOT_YET_RECRUITING","2026-06-09",{"date":31,"type":32},"2026-06-16","ACTUAL",{"date":34,"type":20},"2026-07-01",{"date":36,"type":20},"2027-12-31",{"name":38,"class":39},"Wayne State University","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":16,"minAge":49,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":52,"briefSummary":53,"conditions":54,"keywords":57,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":40},"100513880","verifying-remote-monitoring-effect-on-net-cardiovascular-outcome-remoteverify-rve-100513880","NCT05971225","Verifying Remote Monitoring Effect on Net Cardiovascular Outcome; RemoteVerify (RêVe)","Prospective Multicenter Observation Study on the Association Between Remote Monitoring and Clinical Outcome in Heart Failure Patients (Verifying Remote Monitoring Effect on Net Cardiovascular Outcome; RemoteVerify (RêVe))","ReVe","Inclusion Criteria:\n\n* consented heart failure patients (LVEF\\\u003C=40%) with Biotronik wireless monitoring capable ICD\u002FCRTs aged \\>20 years\n* patients who are new to remote monitoring\n\nExclusion Criteria:\n\n* For patients with a life expectancy of less than 6 months. If patient do not understand the contents of wireless monitoring or it is difficult to fill out the consent form due to cognitive decline.\n\nIf wireless monitoring is performed with a patient enrolled in another clinical trial which remote monitoring may affect the previous enrolled study.","20 Years",{"count":51,"type":20},450,[23],"This study investigates the impact and safety of wireless monitoring on the prognosis of heart failure patients with implanted pacemakers and defibrillators. It aims to examine the frequency of unplanned early hospital visits and the early diagnosis\u002Fintervention of disease exacerbation based on the presence or absence of wireless monitoring. Additionally, the study analyzes the influence of wireless monitoring on the patient's disease progression as well as satisfaction of the study participants.",[55,27,56],"Congestive Heart Failure","Cardiac Resynchronization Therapy",[58,59,27,60],"remote monitoring","congestive heart failure","cardiac resynchronization therapy","RECRUITING","2024-11-28",{"date":64,"type":32},"2024-12-03",{"date":66,"type":32},"2023-11-11",{"date":68,"type":20},"2027-04-30",{"name":70,"class":39},"Saint Vincent's Hospital, Korea",{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":77,"targetDuration":79,"studyType":80,"phases":4,"briefSummary":81,"conditions":82,"keywords":4,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":40},"100325748","luks-leads-registry-on-long-term-performance-of-icd-leads-100325748","NCT03521050","LUKS-Leads Registry on Long-term Performance of ICD Leads","Inclusion Criteria:\n\n* all patients being implanted with a Defibrillator lead from 2006 onwards\n\nExclusion Criteria:\n\n* documented refusal of data collection for scientific purposes",{"count":78,"type":20},1000,"10 Years","OBSERVATIONAL","All patients having an implantable cardiac defibrillator (ICD) implanted and having follow-up at the Cantonal Hospital Lucerne (LUKS), the investigator center, are included in this retrospective ICD lead registry from 2006 onwards. Data is collected prospectively from december 2016 onwards. After certain ICD-leads tended to fail early the investigators aimed for a registry monitoring our patient population with defibrillator leads and evaluating their long-term performance.",[27,83],"Electrical Shock","2020-09-02",{"date":86,"type":32},"2020-09-04",{"date":88,"type":32},"2016-12",{"date":90,"type":20},"2026-12",{"name":92,"class":39},"Luzerner Kantonsspital"]