Torque Device Evaluation

ClinicalTrials.gov ID: NCT07094256

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Official title

Evaluation of Novel Torque Device During Electrophysiology Study Procedure

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID: NCT07094256
Recruitment status: Recruiting
Study type: Interventional
Phase: Not applicable
Lead sponsor: University of Minnesota; Other
Enrollment: 25 participants

Conditions and interventions

Conditions

Interventions

Peritorq Device

Device

Eligibility (public fields only)

Age range: Up to 21 Years
Sex: All
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Aug 25, 2025 (Actual)
Primary completion: Dec 31, 2026 (Estimated)
Completion: Dec 31, 2026 (Estimated)
Last update posted: Aug 6, 2026

2025 – 2026

United States locations

U.S. sites: 2
U.S. states: 2
U.S. cities: 2

Facility	City	State	ZIP	Site status
Children's National	Washington D.C.	District of Columbia	20010	Recruiting
University of Minnesota	Minneapolis	Minnesota	55455	Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT07094256, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Aug 6, 2026 · Synced Nov 15, 2026