[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"electrophysiology-study\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:electrophysiology-study":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,49],{"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":27,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100611924","mobilization-and-outcomes-after-venous-closure-100611924",false,"NCT07246902","Mobilization and Outcomes After Venous Closure","MOVE - Mobilization and Outcomes After VEnous Closure - A Prospective Registry of Real-World Outcomes\u002FUsage\u002FEvidence for the MYNX CONTROL™ VENOUS Vascular Closure Device 6F-12F","MOVE","Inclusion Criteria\n\n1. Able and willing to provide informed consent and to complete a follow-up visit at 14 ± 7 days post-procedure.\n2. Individuals undergoing catheter-based procedures utilizing 6F to 12F inner diameter procedural sheaths, with single or multiple venous access sites in one or both limbs.\n3. Individuals who are candidates to have their venous access site(s) closed with MYNX CONTROL™ VENOUS VCD 6F-12F per IFU.\n4. At the time of enrollment, the Investigator deems the subject a candidate for same-day discharge (SDD) per standard of care (no procedure related events\u002Fcomplications e.g., no new pericardial effusion, post-procedure diuresis not needed, etc.).\n\nExclusion Criteria\n\n1. Presence of bruit, palpable aneurysm, significant candida or groin infection.\n2. Prior to closure, presence of hematoma in the accessed limb.\n3. Currently involved in any other clinical trial that may interfere with the outcomes of this study as determined by the Investigator.\n4. Planned use of other closure devices or techniques other than MYNX CONTROL™ VENOUS VCD 6F-12F.\n5. Life expectancy \\\u003C12 months.","ALL",{"count":19,"type":20},300,"ESTIMATED","14 Days","OBSERVATIONAL","The primary objective of this post-market registry is to collect real-world outcomes and evaluate usage practice of MYNX CONTROL™ VENOUS (MCV) Vascular Closure Device (VCD) 6F-12F in sealing femoral venous access sites in patients who have undergone endovascular procedures in a real-world setting.",[25,26],"Venous Vascular Closure","Electrophysiology Study",[26,28,29,30,25,31,32,33,15,34,35],"Venous closure","Venous access closure","Vascular access closure","Vascular closure device","MYNX CONTROL VENOUS","MOVE Registry","Cardiac Catheterization","MYNX","RECRUITING","2026-03-13",{"date":39,"type":40},"2026-03-16","ACTUAL",{"date":42,"type":40},"2025-11-24",{"date":44,"type":20},"2026-08",{"name":46,"class":47},"Cordis US Corp.","INDUSTRY",3,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":4,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":5},"100600189","torque-device-evaluation-100600189","NCT07094256","Torque Device Evaluation","Evaluation of Novel Torque Device During Electrophysiology Study Procedure","Inclusion Criteria:\n\n* Pediatric patient (≤21 years of age)\n* Undergoing clinically-indicated electrophysiology study and\u002For ablation procedure\n\nExclusion Criteria:\n\n* Adult patient (\\>21 years)","21 Years",{"count":58,"type":20},25,"INTERVENTIONAL",[61],"NA","This study will evaluate the safety and efficacy of a novel catheter torque device after the completion of a clinically-indicated electrophysiology study and\u002For ablation procedure in a pediatric patient. All electrophysiology studies and\u002For ablation procedures will be performed at the discretion of their primary cardiologist and will not be affected by this study protocol. The study protocol will commence once the attending electrophysiologist has completed all necessary intervention and testing and no further evaluation is required.",[26,64],"Ablation","2026-02-19",{"date":67,"type":40},"2026-02-23",{"date":69,"type":40},"2025-08-25",{"date":71,"type":20},"2026-08-04",{"name":73,"class":74},"University of Minnesota","OTHER"]