RecruitingNot ApplicableNCT07094256

Torque Device Evaluation

Evaluation of Novel Torque Device During Electrophysiology Study Procedure


Sponsor

University of Minnesota

Enrollment

25 participants

Start Date

Aug 25, 2025

Study Type

INTERVENTIONAL

Conditions

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

Max Age: 21 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Peritorq for people with ablation and electrophysiology study. The study is currently recruiting participants at 2 locations. People eligible for this study include up to age 21 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEPeritorq

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

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NCT07094256


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