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RECRUITING
NCT07094256
NA

Torque Device Evaluation

Sponsor: University of Minnesota

View on ClinicalTrials.gov

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

Interventions

DEVICE

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