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Clinical Trial Summary

This is an open label, randomized parallel control clinical trial evaluating the efficacy and safety of catheter ablation and surgical ablation in patients with persistent atrial fibrillation with severe atrial fibrosis.


Clinical Trial Description

This is an open label, randomized parallel control clinical trial. Patients with persistent atrial fibrillation with severe atrial fibrosis are 1:1:1 randomized into the group A (circumferential pulmonary vein isolation + linear ablation + bi-atrial mapping + driver ablation), group B (circumferential pulmonary vein isolation + linear ablation + vein of Marshall ethanol infusion) and group C (surgical ablation). Postoperative recurrence rate and other indicators are analyzed to evaluate the efficacy and safety of catheter ablation and surgical ablation in patients with persistent atrial fibrillation with severe atrial fibrosis. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05153486
Study type Interventional
Source Shanghai Chest Hospital
Contact Mu Qin, M.D.
Phone +8613052320103
Email qinmuae@163.com
Status Not yet recruiting
Phase N/A
Start date December 1, 2021
Completion date November 30, 2024

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