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Dapagliflozin Evaluation on Atrial Fibrillation Patients Followed Cox Maze IV Procedure: a cohort study

Dapagliflozin Evaluation on Atrial Fibrillation Patients Followed Cox Maze IV Procedure: a cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300069711
Enrollment
Unknown
Registered
2023-03-23
Start date
2023-03-23
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

atrial fibrillation

Interventions

Dapagliflozin group:N/A
control group:N/A

Sponsors

Beijing Anzhen Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Over 18 years old; 2. Simple surgical CoxMazeIV surgical ablation (simple persistent or long-term persistent atrial fibrillation drug treatment is not effective, and medical catheter ablation fails or is not suitable) 3. Cardiac organic disease combined with persistent or long-term persistent atrial fibrillation requires cardiac surgery and CoxMazeIV surgical ablation; 4. Able and willing to comply with all preliminary and subsequent reviews and requirements; 5. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Dapagliflozin allergy; 2. Hyperthyroidism; 3. Acute myocardial infarction, acute stroke, or other vascular diseases requiring intervention within 6 months before the operation; 4. Received cardiac surgery within 3 months before the surgery; 5. Glomerular filtration rate 65 mm.

Design outcomes

Primary

MeasureTime frame
Recurrence of atrial fibrillation 6 months after surgery;

Secondary

MeasureTime frame
Recurrence of atrial fibrillation 12 months after surgery;Cardiovascular complex adverse events (cardiac death, new heart failure, malignant arrhythmia, stroke);

Countries

China

Contacts

Public ContactXiubin Yang

Beijing Anzhen Hospital, Capital Medical University

xiubinyang@yahoo.com+86 10 6445 6776

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026