[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Kestra Medical Technologies, Inc.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":38},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":21,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":33,"leadSponsor":35,"locationsCount":5},"100449662","assure-wcd-clinical-evaluation---post-approval-study-ace-pas-100449662",false,"NCT05135403","ASSURE WCD Clinical Evaluation - Post Approval Study (ACE-PAS)","ACE-PAS","Inclusion Criteria:\n\n* Adult patient prescribed the ASSURE wearable cardioverter defibrillator\n* Provided written informed consent to participate in the ASSURE Patient Registry\n\nExclusion Criteria:\n\n* Patients who do not meet the Inclusion criteria","ALL","18 Years",{"count":19,"type":20},5179,"ESTIMATED","3 Months","OBSERVATIONAL","Active surveillance study using real-world data collected in the ASSURE Patient Registry. Outcome measures are based on analysis of ASSURE Registry data including data recorded by the WCD then annotated by clinical experts in electrophysiology.",[25],"Sudden Cardiac Arrest","RECRUITING","2025-08-25",{"date":29,"type":30},"2025-09-02","ACTUAL",{"date":32,"type":30},"2021-11-20",{"date":34,"type":20},"2025-10-01",{"name":36,"class":37},"Kestra Medical Technologies, Inc.","INDUSTRY",""]