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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

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Conditions

Electrophysiology StudyAblation

Locations

Children's National

Washington D.C., District of Columbia 20010

United States

University of Minnesota

Minneapolis, Minnesota 55455

United States