This prospective, randomized, controlled trial is designed to compare the safety and efficacy of remote magnetic navigation-guided ablation for ventricular premature complexes arising from non-outflow tracts with manual control navigation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
200
Catheter Ablation with RMN and MCN
Freedom rate of PVC
Efficacy endpoint
Time frame: one year
Procedure-related Complications
Safety endpoint
Time frame: one year
fluoroscopic time
Time frame: one day
ablation time
Time frame: one day
procedure time
Time frame: one day
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