[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Medtronic Cardiac Surgery\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":87},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,39,65],{"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":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":38},"100381033","medtronic-symbiosis-post-market-registry-for-patients-undergoing-cardiac-surgery-100381033",false,"NCT04241328","Medtronic SYMBIOSIS Post-Market Registry for Patients Undergoing Cardiac Surgery","SYMBIOSIS Post-Market Registry","SYMBIOSIS","Inclusion Criteria:\n\n* Subject or legally authorized representative provides written data release and\u002For informed consent per institution and\u002For geographical requirements prior to discharge from participating registry hospital.\n* Subject will undergo or underwent a procedure in which an eligible Medtronic CS product is\u002Fwas used.\n\nExclusion Criteria:\n\n* Currently participating in an interventional drug or device study which may induce confounding factor(s) to the results from this Registry","ALL",{"count":19,"type":20},5000,"ESTIMATED","30 Days","OBSERVATIONAL","The purpose of this observational, multi-center prospective, post-market registry is to confirm real-world device safety and performance, to ensure the continued acceptability of identified risks, and detect emerging risks.",[25],"Cardiovascular Diseases","RECRUITING","2026-06-08",{"date":29,"type":30},"2026-06-09","ACTUAL",{"date":32,"type":30},"2020-01-09",{"date":34,"type":20},"2026-12-31",{"name":36,"class":37},"Medtronic Cardiac Surgery","INDUSTRY",14,{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":4,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":17,"minAge":46,"maxAge":4,"enrollmentInfo":47,"targetDuration":4,"studyType":49,"phases":50,"briefSummary":52,"conditions":53,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":56,"lastUpdatePostDateStruct":57,"startDateStruct":59,"completionDateStruct":61,"leadSponsor":63,"locationsCount":64},"100327687","medtronic-terminate-af-study-100327687","NCT03546374","Medtronic Terminate AF Study","Irrigated Radio Frequency Ablation to Terminate Non-Paroxysmal Atrial Fibrillation (Terminate AF Study)","Inclusion Criteria:\n\n* History of non-paroxysmal AF (persistent or longstanding persistent)\n* Concomitant indication for non-emergent open-heart surgery, eg,\n\n  1. Coronary artery bypass grafting\n  2. Valve repair or replacement\n* Able to take the anticoagulant warfarin or novel oral anticoagulants (NOAC)\n\nExclusion Criteria:\n\n* Wolff-Parkinson-White syndrome\n* New York Heart Association (NYHA) Class = IV\n* Left Ventricular Ejection Fraction ≤ 30%\n* Need for emergent cardiac surgery (ie, cardiogenic shock) or redo open heart surgery\n* Previous AF ablation, atrioventricular (AV) -nodal ablation, or surgical Maze procedure\n* Contraindication for anticoagulation therapy\n* Left atrial diameter \\> 6.0 cm\n* Preoperative need for an intra-aortic balloon pump or intravenous inotropes\n* Renal failure requiring dialysis or hepatic failure\n* Life expectancy of less than 1 year\n* Predicted risk of operative mortality \\>10% as assessed by STS Risk Calculator\n* Pregnancy or desire to be pregnant within 12 months of the study treatment\n* Current diagnosis of active systemic infection\n* Active endocarditis\n* Documented MI 30 days prior to study enrollment\n* Current or planned participation in an investigational or observational drug or device trial related to the treatment of atrial arrhythmias","18 Years",{"count":48,"type":20},160,"INTERVENTIONAL",[51],"NA","The purpose of this study is to demonstrate the safety and effectiveness of the Cardioblate iRF and CryoFlex hand held devices for the treatment of non-paroxysmal atrial fibrillation (AF).",[54,55],"Persistent Atrial Fibrillation","Longstanding Persistent Atrial Fibrillation","2026-05-07",{"date":58,"type":30},"2026-05-14",{"date":60,"type":30},"2018-11-15",{"date":62,"type":20},"2026-12",{"name":36,"class":37},15,{"id":66,"slug":67,"hasResults":11,"nctId":68,"briefTitle":69,"officialTitle":70,"acronym":4,"eligibilityCriteria":71,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":72,"targetDuration":74,"studyType":22,"phases":4,"briefSummary":75,"conditions":76,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},"100368139","medtronic-cardiac-surgery-pmcf-registry-100368139","NCT04073420","Medtronic Cardiac Surgery PMCF Registry","Medtronic Cardiac Surgery Post Market Clinical Follow-up Registry","Inclusion Criteria:\n\n1. Patient or legally authorized representative provides written authorization and\u002For consent per institution and geographical requirements\n2. Patient has or is intended to receive or be treated with an eligible product\n3. Patient is within enrollment window of treatment\u002Ftherapy received at the time of their initial Registry enrollment, or meets criteria for retrospective enrollment\n\nExclusion Criteria:\n\n1. Patient who is, or is expected to be, inaccessible for follow-up\n2. Patient prohibited from participation by local law\n3. Patient is currently enrolled in or plans to enroll in any concurrent investigational drug and\u002For device study that may confound results",{"count":73,"type":20},2700,"10 Years","This registry is being conducted to support ongoing post-market surveillance activities.",[77],"Valve Disease, Heart","2026-04-08",{"date":80,"type":30},"2026-04-13",{"date":82,"type":30},"2019-12-02",{"date":84,"type":20},"2039-12-31",{"name":36,"class":37},26,""]