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Empagliflozin effect on supraventricular arrhythmias

Phase 3
Recruiting
Conditions
Supraventricular arrhythmias.
Atrial fibrillation and flutter
Registration Number
IRCT20240116060704N1
Lead Sponsor
Bagheiat-allah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
30
Inclusion Criteria

Age more than 18 years
Diagnosis of heart failure based on echocardiography
Having an ICD for more than 3 months before starting participation in the study
Obtaining the patient's informed consent

Exclusion Criteria

Using SGLT2 inhibitors before starting participation in the study
New York Heart Association function class IV heart failure
Renal dysfunction (eGFR < 20 mL/min/1.73 m2 ) or dialysis
Hepatic dysfunction (AST or ALT > 3 times higher than upper limit of normal)
Body mass index < 18.5 kg/m2
Pregnancy or lactation
Patients with the following events within 3 months before the eligibility test: alteration of the anti-arrhythmic drug, catheter ablation for supraventricular arrhythmia, coronary revascularization, open-heart surgery, development of coronary artery disease, stroke or transient ischemic stroke, seizure, infection requiring hospitalization
Other commodities, including various infections, major surgery, type 1 diabetes, pituitary or adrenal insufficiency, cancer
Single chamber ICDs or ICDs unable to record atrial arrhythmias

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Frequency of the supraventricular arrhythmias (atrial fibrillation and flutter). Timepoint: During the three months before the intervention and during the three months after the intervention. Method of measurement: ICD (implantable cardioverter-defibrillator) record.
Secondary Outcome Measures
NameTimeMethod
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