Atrial fibrillation
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients who have agreed to this study in the document 2) Patients aged 18 to 80 3) Patients with persistent atrial fibrillation with a duration of 1 week or more with drug resistance or wish for catheter ablation 4) Patients with a left atrium diameter of 55 mm or less 5) Patients with a left ventricular ejection fraction of over 45%
Exclusion criteria
Exclusion criteria: 1) Patients with contraindications to anticoagulant therapy or unable to undergo catheter ablation due to cardiac thrombosis 2) Patients who have previously undergone catheter ablation for atrial fibrillation 3) Patients with a postprecedural follow-up period of less than six months 4) Patients with moderate or severe mitral or aortic valve valvular disease (regurgitation/stenosis) 5) Patients with hypertrophic cardiomyopathy 6) Patients with a history of myocardial infarction 7) Patients after transplantation of cardiac implantable electronic device 8) Patients for whom this study is not indicated because of other reasons (e.g., patients considered to be anatomically difficult to use CARTOFINDER)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Survival free rate from atrial tachyarrhythmia recurrence during 12 months follow-up after the index ablation | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Procedural detail data including procedure time and complications 2. Relationship between left atrial low voltage area and atrial tachyarrhythmia recurrence rate after additional ablation to localized atrial fibrillation sources plus conventional pulmonary vein isolation and ablation of non-pulmonary vein foci 3. Change of left atrial function before and six months after the index ablation between two groups | — |
Countries
Japan
Contacts
Sakakibara heart institute Cardiology