[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100600189":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":25,"locations":30,"responsibleParty":64,"collaborators":20,"id":66,"slug":20,"hasResults":67,"nctId":68,"briefTitle":69,"officialTitle":70,"acronym":20,"eligibilityCriteria":71,"healthyVolunteers":67,"sex":72,"minAge":20,"maxAge":73,"enrollmentInfo":74,"targetDuration":20,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":20,"overallStatus":33,"whyStopped":20,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":93},{"fullName":5,"class":6},"University of Minnesota","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Torque Device","EXPERIMENTAL","After the completion of the electrophysiology study and\u002For ablation procedure, the catheters remain in the intra-cardiac locations. While in place, measurements will be obtained from each catheter. Once the baseline measurements have been obtained, the Peritorq device will be placed onto each relevant catheter. Once secured, all measurements will be repeated with each catheter at the identical location. After measurements have been obtained, the operator will perform minor catheter movements to note subjective maneuverability and stability of the catheter with the torque device in place",[13],"Device: Peritorq",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","Peritorq","Novel torque device specifically designed for electrophysiology and ablation catheters",[9],null,[22],{"name":23,"affiliation":5,"role":24},"Bradley Clark","PRINCIPAL_INVESTIGATOR",[26],{"name":23,"role":27,"phone":28,"phoneExt":20,"email":29},"CONTACT","(612) 626-2755","clarkb@umn.edu",[31,50],{"facility":32,"status":33,"city":34,"state":35,"zip":36,"country":37,"countryCode":38,"cosmosGeoPoint":39,"geoPoint":44,"contacts":45},"Children's National","RECRUITING","Washington D.C.","District of Columbia","20010","United States","US",{"type":40,"coordinates":41},"Point",[42,43],-77.03637,38.89511,{"lat":43,"lon":42},[46],{"name":47,"role":27,"phone":48,"phoneExt":20,"email":49},"Charles Berul","202-476-4132","CBerul@childrensnational.org",{"facility":5,"status":33,"city":51,"state":52,"zip":53,"country":37,"countryCode":38,"cosmosGeoPoint":54,"geoPoint":58,"contacts":59},"Minneapolis","Minnesota","55455",{"type":40,"coordinates":55},[56,57],-93.26384,44.97997,{"lat":57,"lon":56},[60],{"name":61,"role":27,"phone":62,"phoneExt":20,"email":63},"Erick Jimenez","612-626-2830","jimen191@umn.edu",{"type":65,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100600189",false,"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)","ALL","21 Years",{"count":75,"type":76},25,"ESTIMATED","INTERVENTIONAL",[79],"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.",[82,83],"Electrophysiology Study","Ablation","2026-02-19",{"date":86,"type":87},"2026-02-23","ACTUAL",{"date":89,"type":87},"2025-08-25",{"date":91,"type":76},"2026-08-04",{"name":5,"class":6},2]