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Recruiting Phase 4

Clinical Impact of SGLT2 Inhibitor After DC Cardioversion in Persistent AF With HFpEF

NCT07776054 · tracked via the Priya Life Science South Korea tracker
Phase
Phase 4
Started
2024-02-01
Last updated
2026-08-20

Condition(s) studied

Atrial FibrillationSGLT2 InhibitorDC Cardioversion

Investigational drug(s) / intervention(s)

SGLT2 inhibitors (Dapagliflozin and Empagliflozin)

SGLT2 inhibitors (Dapagliflozin and Empagliflozin): Patients receive an SGLT2 inhibitor (empagliflozin or dapagliflozin) after successful DC cardioversion, in addition to guideline-directed anticoagulation and antiarrhythmic drugs for 1 month.

Study summary

SGLT2 inhibitors improve outcomes in heart failure across the ejection fraction spectrum, but their effect on maintenance of sinus rhythm after rhythm-control therapy is largely unknown. This prospective, single-center, open-label randomized controlled trial evaluates whether an SGLT2 inhibitor started after successful electrical cardioversion reduces recurrence of atrial tachyarrhythmia at 1 month in patients with persistent atrial fibrillation and heart failure with preserved ejection fraction. 200 patients will be randomized 1:1 to receive an SGLT2 inhibitor or no SGLT2 inhibitor.

Eligibility

Sex
ALL
Min age
19 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥19 years * Persistent atrial fibrillation * H2FPEF score ≥6 or HFA-PEFF score ≥5 * Restoration of sinus rhythm after electrical cardioversion Exclusion Criteria: * Previous use of an SGLT2 inhibitor * Intracardiac thrombus on transesophageal echocardiography * Refusal to participate

Primary outcome measure(s)

  • Recurrence of atrial tachyarrhythmia — 1 month after randomization (±1 week)
    Composite of atrial fibrillation, atrial flutter, and atrial tachycardia, documented on 12-lead ECG or as an episode lasting ≥30 seconds on continuous ECG monitoring.

Trial sites (1)

FacilityCityRegionStatus
Samsung Medical Center Seoul Seoul Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07776054 on ClinicalTrials.gov ↗ ← All trials in South Korea