NCT07094256NARecruiting
Torque Device Evaluation
University of Minnesota
Start Date
8/25/2025
Completion Date
8/4/2026
Summary
This study will evaluate the safety and efficacy of a novel catheter torque device after the completion of a clinically-indicated electrophysiology study and/or ablation procedure in a pediatric patient. All electrophysiology studies and/or 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.
Eligibility Criteria
Age Range: No minimum to 21 years
Inclusion Criteria:
* Pediatric patient (≤21 years of age)
* Undergoing clinically-indicated electrophysiology study and/or ablation procedure
Exclusion Criteria:
* Adult patient (\>21 years)
Interventions
DEVICE
Peritorq
Conditions
Electrophysiology StudyAblation
Locations
Children's National
Washington D.C., District of Columbia 20010
United States
University of Minnesota
Minneapolis, Minnesota 55455
United States