Home › NCT07094256
Torque Device Evaluation
Evaluation of Novel Torque Device During Electrophysiology Study Procedure
Who can join
Up to age 21 · All sexes
Full eligibility criteria
Inclusion Criteria: * Pediatric patient (≤21 years of age) * Undergoing clinically-indicated electrophysiology study and/or ablation procedure Exclusion Criteria: * Adult patient (\>21 years)
About the study
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.
What is being tested
- Peritorq (device)
Sponsor: University of Minnesota · Participants: 25 · Started: Aug 25, 2025
Contact the study team
- Bradley Clark · Phone: (612) 626-2755
Official record on ClinicalTrials.gov — NCT07094256
Locations in the U.S.
| District of Columbia | Children's National, Washington D.C. |
| Minnesota | University of Minnesota, Minneapolis |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.