Efficacy of Dapagliflozin on Recurrence After Catheter Ablation for Atrial Fibrillation

NCT ID: NCT06433479

Last Updated: 2025-07-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 200 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-07-15
• Study Completion Date: 2025-07-01

Brief Summary

This is a single-center, parallel-group, randomized, open-label trial evaluating the effect of 3-month treatment with dapagliflozin 10mg once daily on the recurrence of atrial fibrillation after catheter ablation for atrial fibrillation in patients without diabetes, heart failure, or chronic kidney disease.

Detailed Description

Atrial fibrillation (AF) is one of the most common arrhythmias. Catheter ablation of atrial fibrillation, as the main means of rhythm control, can effectively maintain sinus rhythm, reduce the recurrence of AF burden, and improve the patient's quality of life and prognosis. However, AF recurrence still occurs in 30-50% of patients after atrial fibrillation catheter ablation, and there is currently no effective strategy to reduce the recurrence rate after atrial fibrillation ablation.

Sodium-glucose cotransporter 2 inhibitors (SGLT2i) are a new class of diabetic drugs and large clinical trials have established their multiple cardiovascular benefits. Several studies demonstrated that SGLT2i might reduce AF/atrial flutter events among patients with diabetes. Our cohort study and meta-analysis demonstrated a lower risk of AF recurrence with the use of SGLT2i among patients with diabetes after AF ablation. However, the beneficial effects of SGLT2i in patients after AF catheter ablation without current indications for SGLT2i were uncertain.

In this study, we aim to evaluate the effect of dapagliflozin on AF burden. Patients with persistent AF undergoing initial catheter ablation without diabetes at high cardiovascular risk, heart failure, or chronic kidney disease will be enrolled. Patients will be randomly assigned to either the dapagliflozin group (10mg/d) for 3 months or the control group stratified according to body mass index (<24, ≥24kg/m2) or left atrial diameter (<45，≥45mm).

The primary outcome is atrial fibrillation burden calculated as the percentage of of all atrial arrhythmia episodes detected by 7-day single-lead ECG patches at 3 months after ablation. Quality of life and echocardiography changes of left atrial structure will also be evaluated at 3 months. Our central hypothesis is that SGLT2i will reduce the AF burden after catheter ablation.

Conditions

Atrial Fibrillation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Dapagliflozin

Dapagliflozin 10 mg per day for 3 months after initial catheter ablation

Group Type: EXPERIMENTAL

Dapagliflozin 10 mg per day for 3 months after initial catheter ablation

Intervention Type: DRUG

Dapagliflozin 10 mg per day for 3 months after initial catheter ablation

Control

No intervention

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Dapagliflozin 10 mg per day for 3 months after initial catheter ablation

Dapagliflozin 10 mg per day for 3 months after initial catheter ablation

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. age between 18-80 years

2. diagnosed with persistent atrial fibrillation based on ECG or Holter

3. planned initial catheter ablation for atrial fibrillation

4. have the capacity to understand and sign an informed consent form.

Exclusion Criteria

1. diagnosed with persistent atrial fibrillation longer than 5 years or left atrial anterior-posterior diameter ≥ 50mm

2. diagnosed with atrial fibrillation secondary to reversible causes (such as hyperthyroidism, acute infection, etc.)

3. severe structural heart disease (hypertrophic cardiomyopathy, rheumatic heart disease, dilated cardiomyopathy, etc.)

4. currently take sodium-glucose co-transporter 2 inhibitors

5. have the following Class I indications for sodium-glucose co-transporter 2 inhibitors: i. type 2 diabetes ii. history of heart failure (HF), including HF with reduced ejection fraction, mildly reduced ejection fraction, and preserved ejection fraction iii. chronic kidney disease with eGFR=20-60 ml/min/1.73m2

6. have the following contraindication of sodium-glucose co-transporter 2 inhibitors: i. previous allergic reactions to dapagliflozin ii. end-stage renal failure or dialysis

7. type 1 diabetes, or previous diabetic ketoacidosis

8. severe hypoglycemia or genitourinary infection in the past 12 months

9. hypovolemia or hypotension

10. planned surgery or other interventional procedure within 3 months

11. other arrhythmias mandating anti-arrhythmic drug therapy

12. have intracardiac thrombus

13. active infection

14. unable to give informed consent

15. women of childbearing potential

16. currently enrolled in another clinical study

17. other condition unsuitable to participate in this study judged by investigators

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Beijing Anzhen Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Beijing Anzhen Hospital

Beijing, Beijing Municipality, China

Countries

China

Other Identifiers

2024-4-20610

Identifier Type: -

Identifier Source: org_study_id