[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100605002":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":7,"centralContacts":8,"locations":7,"responsibleParty":14,"collaborators":7,"id":18,"slug":19,"hasResults":20,"nctId":21,"briefTitle":22,"officialTitle":22,"acronym":23,"eligibilityCriteria":24,"healthyVolunteers":20,"sex":25,"minAge":26,"maxAge":7,"enrollmentInfo":27,"targetDuration":30,"studyType":31,"phases":7,"briefSummary":32,"conditions":33,"keywords":35,"overallStatus":38,"whyStopped":7,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":7},{"fullName":5,"class":6},"AZ Sint-Jan AV","OTHER",null,[9],{"name":10,"role":11,"phone":12,"phoneExt":7,"email":13},"Emma Christiaen","CONTACT","+32 50 45 32 93","SM-SJ-Cardiologie-Studies@azsintjan.be",{"type":15,"investigatorFullName":16,"investigatorTitle":17,"investigatorAffiliation":5,"oldNameTitle":7,"oldOrganization":7},"PRINCIPAL_INVESTIGATOR","Jean-Benoît Le Polain de Waroux","Coordinating Principal Investigator","100605002","observational-belgian-registry-of-implanted-ev-icd-to-evaluate-parameters-and-complications-of-the-new-device-in-real-world-settings-100605002",false,"NCT07156851","Observational BELgian Registry of Implanted EV-ICD to Evaluate Parameters and Complications of the New Device in Real World Settings","BELIEVE","Inclusion Criteria:\n\n* At least 18 years old\n* Previous or planned EV-ICD implantation (successful or not)\n* Informed consent signed\n\nExclusion Criteria:\n\n* Patients who did not undergo any step of the implantation procedure","ALL","18 Years",{"count":28,"type":29},100,"ESTIMATED","15 Years","OBSERVATIONAL","The goal of this observational study is to follow all patients implanted with extravascular implantable cardioverter-defibrillators (EV-ICDs) in Belgium throughout the lifetime of the devices. The main goal of the study is to keep track of:\n\n* all parameters of the device\n* complications\n* arrhythmia detection and therapy delivery\n* clinical endpoints (quality of life, cardiac and infectious events) Participants who underwent or will undergo an EV-ICD implantation as part of their regular medical care will be asked if data can be collected from their medical record. No additional tasks are required for the study.",[34],"Implantable Cardioverter Defibrillator (ICD)",[36,37],"Extravascular implantable cardioverter-defibrillator","EV-ICD","NOT_YET_RECRUITING","2025-08-27",{"date":41,"type":42},"2025-09-05","ACTUAL",{"date":44,"type":29},"2025-11",{"date":46,"type":29},"2040-07-01",{"name":5,"class":6}]