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Efficacy of Finerenone on Recurrence After Catheter Ablation for Atrial Fibrillation: FINE-AF trial

Efficacy of Finerenone on Recurrence After Catheter Ablation for Atrial Fibrillation: FINE-AF trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600131231
Enrollment
Unknown
Registered
2026-08-31
Start date
2026-09-01
Completion date
Unknown
Last updated
2026-09-07

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

Conditions

persistent atrial fibrillation

Interventions

Sponsors

Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18–80 years; 2. Diagnosed with persistent atrial fibrillation confirmed by ambulatory electrocardiogram or standard 12-lead electrocardiogram; 3. Scheduled for first-time catheter ablation for atrial fibrillation; 4. Able to understand and provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Duration of persistent atrial fibrillation >5 years, or echocardiography demonstrating left atrial anteroposterior diameter >=50 mm; 2. Atrial fibrillation secondary to reversible causes (e.g., hyperthyroidism, acute infection, post-cardiac surgery); 3. Presence of severe structural heart disease (e.g., hypertrophic cardiomyopathy, rheumatic valvular heart disease, dilated cardiomyopathy); 4. Current use of any mineralocorticoid receptor antagonist (MRA) (e.g., spironolactone, eplerenone, or finerenone); 5. Class I indication for finerenone: chronic kidney disease (CKD) associated with type 2 diabetes and albuminuria; 6. Contraindications or high-risk features for finerenone: (1) Baseline serum potassium >5.0 mmol/L; (2) Severe renal impairment (eGFR <25 mL/min/1.73m^2) or patients with end-stage renal disease on dialysis; (3) Severe hepatic impairment (Child-Pugh class C); (4) Addison's disease; (5) Concomitant use of strong CYP3A4 inhibitors (e.g., itraconazole, clarithromycin, etc.); 7. Severe hypotension (systolic blood pressure <90 mmHg) or hypovolemia; 8. Planned major other surgery within 3 months; 9. Presence of thrombus in the left atrium / left atrial appendage; 10. Pregnant women, or women of childbearing potential who may become pregnant without effective contraception.

Design outcomes

Primary

MeasureTime frame
Change in atrial fibrillation burden at 3 months after catheter ablation;

Secondary

MeasureTime frame
Changes in left atrial anterior posterior diameter, LVEF and other echocardiographic indicators;Overall atrial fibrillation recurrence rate;Composite endpoint of hospitalization or cardiovascular death due to cardiovascular reasons;AFEQT Quality of Life Score;First recurrence of atrial tachycardia;

Countries

China

Contacts

Public ContactWenzhi Shen

Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University

swz2588@163.com+86 25 83106666

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026