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Driver Ablation of Persistent Atrial Fibrillation With Severe Atrial Fibrosis.

A Randomized Control Study of Driver Ablation of Persistent Atrial Fibrillation With Severe Atrial Fibrosis: a Chinese Registry Study.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05085912
Enrollment
300
Registered
2021-10-20
Start date
2021-11-01
Completion date
2024-10-31
Last updated
2021-10-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Persistent Atrial Fibrillation

Keywords

persistent atrial fibrillation, severe atrial fibrosis, driver ablation

Brief summary

This is an open label, randomized parallel control clinical trial, to demonstrate the role of driver mechanism in maintenance substrate of persistent atrial fibrillation with severe atrial fibrosis, and evaluate the clinical outcomes of driver mapping and ablation strategy in patients with persistent atrial fibrillation with severe atrial fibrosis.

Detailed 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 group A (circumferential pulmonary vein isolation + linear ablation + bi-atrial mapping + driver ablation), group B (circumferential pulmonary vein isolation + linear ablation + posterior wall box isolation) and group C (circumferential pulmonary vein isolation + linear ablation + vein of Marshall ethanol infusion). Postoperative recurrence rate and other indicators are analyzed to demonstrate the role of driver mechanism in maintenance substrate of persistent atrial fibrillation with severe atrial fibrosis and evaluate the clinical outcomes of driver mapping and ablation strategy in patients with persistent atrial fibrillation with severe atrial fibrosis.

Interventions

Patients receive circumferential pulmonary vein isolation and linear ablation (ablation of a roof line and a mitral isthmus line) combined with bi-atrial mapping and driver ablation.

PROCEDURECircumferential pulmonary vein isolation + linear ablation + posterior wall box isolation

Patients receive circumferential pulmonary vein isolation and linear ablation (ablation of a roof line and a mitral isthmus line) combined with posterior wall box isolation.

Patients receive circumferential pulmonary vein isolation and linear ablation (ablation of a roof line and a mitral isthmus line) combined with vein of Marshall ethanol infusion.

Sponsors

Shanghai Chest Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Aged 18 to 80 years old; 2. Persistent AF with severe atrial fibrosis; 3. Nonresponse or intolerance to ≥1 antiarrhythmic drug.

Exclusion criteria

1. With uncontrolled congestive heart failure; 2. Having significant valvular disease; 3. With myocardial infarction or stroke within 6 months of screening; 4. With Significant congenital heart disease; 5. Ejection fraction was \<40% measured by echocardiography; 6. Allergic to contrast media; 7. Contraindication to anticoagulation medications; 8. Severe pulmonary disease e.g. restrictive pulmonary disease, chronic obstructive disease (COPD); 9. Left atrial (LA) thrombus; 10. Having any contraindication to right or left sided heart catheterization; 11. Previous atrial fibrillation ablation; 12\. Presence of an implanted cardioverter-defibrillator; 13. Previous history of cardiac surgery; 14. Poor general health; 15. Life expectancy less than 6 months.

Design outcomes

Primary

MeasureTime frameDescription
Postoperative atrial fibrillation (AF)/atrial flutter (AFL)/atrial tachycardia (AT) recurrence rateup to 12 months after ablationAF/AFL/AT recurrence is defined as presence of documented AF/AFL/AT episodes of 30 seconds or longer duration
Intraoperative AF termination ratethrough ablation completion, an average of 3 hoursAF termination is defined as conversion to sinus rhythm or stable AFL/AT.

Secondary

MeasureTime frameDescription
Incidence of complicationsup to 12 months after ablationdeath, atrioesophageal fistula, cardiac tamponade/perforation, myocardial infarction, stroke/cerebrovascular accident, thromboembolism, diaphragmatic paralysis, pneumothorax, heart block, pulmonary vein stenosis, pulmonary edema, pericarditis and major vascular access complication or bleeding
Postoperative AF recurrence rateup to 12 months after ablationAF recurrence is defined as presence of documented AF episodes of 30 seconds or longer duration
Changes in the left ventricular ejection fractionup to 12 months after ablationChanges in the left ventricular ejection fraction
Changes in the diameter of the left atriumup to 12 months after ablationChanges in the diameter of the left atrium
Postoperative AFL/AT rateup to 12 months after ablationoccurrence of AFL/AT is defined as presence of documented AFL/AT episodes of 30 seconds or longer duration

Contacts

Primary ContactMu Qin, M.D.
qinmuae@163.com+8613052320103

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026