Status: Not yet recruiting
PulseMagic™ TrueForce™ PAF NMPA Study
This clinical investigation is intended to demonstrate safety and effectiveness of the PulseMagic™ TrueForce™ Ablation Catheter and the PulseMagic™Pulse Field Ablation (PFA) Generator, and Columbus™ 3D EP Navigation System with Pulsed Field Ablation Software for the treatment of symptomatic, recurrent, drug refractory paroxysmal atrial fibrillation (PAF).
Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Shanghai MicroPort EP MedTech Co., Ltd.Updated: Jul 22, 2026Locations: 1
Eligibility criteria
Aged ≥ 18 years old. [+4]
Patients with a history of atrial fibrillation ablation. [+9]