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Torque Device Evaluation
Sponsor: University of Minnesota
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.
Official title: Evaluation of Novel Torque Device During Electrophysiology Study Procedure
Key Details
Gender
All
Age Range
Any - 21 Years
Study Type
INTERVENTIONAL
Enrollment
25
Start Date
2025-08-25
Completion Date
2026-08-04
Last Updated
2026-02-23
Healthy Volunteers
No
Conditions
Interventions
Peritorq
Novel torque device specifically designed for electrophysiology and ablation catheters
Locations (2)
Children's National
Washington D.C., District of Columbia, United States
University of Minnesota
Minneapolis, Minnesota, United States