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 Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
25
Novel torque device specifically designed for electrophysiology and ablation catheters
University of Minnesota
Minneapolis, Minnesota, United States
RECRUITINGDifference in Impedance
Obtained from catheter at baseline and after Peritorq device placed
Time frame: 15 minutes
Difference in Sensing of Chamber Amplitude (mV)
Obtained from catheter at baseline and after Peritorq device placed
Time frame: 15 minutes
Difference in Capture Threshold of Atrium and Ventricle (mA)
Obtained from catheter at baseline and after Peritorq device placed
Time frame: 15 minutes
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