NCT07094256

Torque Device Evaluation

Evaluation of Novel Torque Device During Electrophysiology Study Procedure

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 25 (estimated)
• Sponsor: University of Minnesota · Academic / Other
• Sex: All
• Age: 21 Years
• Healthy volunteers: Not accepted

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.

Conditions

• Electrophysiology Study
• Ablation

Interventions

Type	Name	Description
DEVICE	Peritorq	Novel torque device specifically designed for electrophysiology and ablation catheters

Timeline

• Start date: 2025-08-25
• Primary completion: 2026-08-04
• Completion: 2026-08-04
• First posted: 2025-07-30
• Last updated: 2026-02-23

Locations

2 sites across 1 country: United States

Regulatory

• FDA-regulated device study