Torque Device Evaluation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeUp to 21
SponsorUniversity of Minnesota

About this trial

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 criteria

Qualifiers

Pediatric patient (≤21 years of age)

Undergoing clinically-indicated electrophysiology study and/or ablation procedure

Disqualifiers

Adult patient (>21 years)

Trial design

Treatments tested in this trial

  • Peritorq

Treatment groups

25 Participants
are divided into 1 treatment group

Sponsors and collaborators