Clinical Trial

Workflow Optimization During Pulse Field Ablation for Atrial Fibrillation

Study acronym: PFA_workflow
Not Yet Recruiting Phase 4
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Summary
To evaluate the efficacy and safety of intravenous lidocaine in reducing diaphragmatic contraction and suppressing the cough reflex during pulsed field ablation procedures.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-01-14.
Trial Details
NCT Number NCT07354217
Lead Sponsor National Taiwan University Hospital
Collaborators: Johnson & Johnson
Conditions Pulsed Field Ablation, Lidocaine
Enrollment 60 participants
Start Date 2026-06-01
Primary Completion 2030-12-31 (estimated)
Study Completion 2030-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-04-20