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Effect of Dapagliflozin on the occurrence of Atrial fibrillation rhythm

Studying the effect of Dapagliflozin on the occurrence of Atrial fibrillation rhythm after coronary artery bypass graft surgery in a clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241121063794N1
Enrollment
83
Registered
2025-04-08
Start date
2025-04-21
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Post operative Atrial fibrilation.

Interventions

Intervention 1: "Intervention group:" Dapagliflozin recipients who underwent echocardiography during hospitalization and were treated with dapagliflozin 10 mg (Medava Pharmaceutical Company) daily for

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult patients over 18 years Patients who have given informed consent Sinus rhythm before surgery

Exclusion criteria

Exclusion criteria: History of diabete Need for emergency CABG Contraindication for dapagliflozin History of SGLT2in use before hospitalization History of thyroid problem Need for simultaneous valve surgery Previous history of heart surgery History of congenital heart disease History of atrial fibrillation rhythm before hospitalization History of pacemaker implantation

Design outcomes

Primary

MeasureTime frame
Post-operative atrial fibrillation (POAF) is one of the most important complications of cardiac surgery, which can increase morbidity and mortality, increase length of stay, and cost of treatment, and can also lead to dangerous consequences such as heart attack, acute renal infarction, congestive heart failure, and even death for the patient. Timepoint: To assess AF rhythm, patients are monitored 24 hours a day in the cardiac surgery intensive care unit with 24-hour monitoring, on the second day in the ward with ECG every 8 hours or when the patient becomes symptomatic and ECG is taken on the third day with 24-hour Holter monitoring (given the maximum incidence of AF on the third day), and on the fourth day with ECG. Method of measurement: Holter heart rhythm Electrocardiogram.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamid Nobakht

Tehran University of Medical Sciences

Hamid79.hn@gmail.com+98 937 184 6437

Outcome results

None listed

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