[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Universitätsklinikum Köln\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":66},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":5},"100575393","s-icd-implantation-us-based-pilot-study-100575393",false,"NCT06771700","S-ICD Implantation: US Based Pilot Study","Feasibility of an Intra-operative and Non-fluoroscopic Subcutaneous ICD Positioning and Assessment of the PRAETORIAN Score During Implantation: a Pilot Study","SUSTAIN S-ICD","Inclusion Criteria:\n\n* consecutive patients presenting for S-ICD implantation at our institution\n\nExclusion Criteria:\n\n* patients unable to consent.\n* pregnancy","ALL",{"count":19,"type":20},20,"ESTIMATED","INTERVENTIONAL",[23],"NA","This trial investigates two key aspects of the S-ICD implantation process. 1) For S-ICD implantation a pre-operative x-ray-based assessment of the anatomy and location of the heart is required. This study seeks to investigate the feasibility of US to potentially replace the need for x-ray 2) The PRAETORIAN score predicts defibrillation test success in subcutaneous ICD implantation but can only be calculated after the procedure. This pilot study aims to evaluate the feasibility of US determining the PRAETORIAN score intraoperatively. Lead-to-sternum distance and generator position measurments during the implantation procedure will be evaluated. Twenty consecutive patients scheduled for S-ICD implantation will be enrolled. The study involves no deviation from standard implantation procedures and requires no follow-up beyond standard post-operative chest X-ray on day one.",[26],"Sudden Cardiac Death",[28,29],"S-ICD","Defibrillator","RECRUITING","2025-07-03",{"date":33,"type":34},"2025-07-09","ACTUAL",{"date":36,"type":34},"2025-03-01",{"date":38,"type":20},"2025-11-01",{"name":40,"class":41},"Universitätsklinikum Köln","OTHER",{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":17,"minAge":49,"maxAge":50,"enrollmentInfo":51,"targetDuration":4,"studyType":53,"phases":4,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":65},"100545934","investigation-of-the-audible-icd-alert-tone-100545934","NCT06388382","Investigation of the Audible ICD Alert Tone","Investigation of the Audible Alert Tone in ICD Patients with Subcutaneous Cardioverter Defibrillators","Inclusion Criteria:\n\n* patient equipped with a subcutaneous ICD\n* willing to participate\n\nExclusion Criteria:\n\n* S-ICD implantation within the past 3 weeks\n* patient is deaf","15 Years","100 Years",{"count":52,"type":20},150,"OBSERVATIONAL","Ability of ICD patients to hear the audible ICD alert is being assessed.",[56],"Implantable Defibrillator User","2024-11-06",{"date":59,"type":34},"2024-11-08",{"date":61,"type":34},"2024-10-01",{"date":63,"type":20},"2025-05-30",{"name":40,"class":41},1,""]