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The effect of Empagliflozin on outcomes of patients with myocardial infarction undergoing primary PCI

Phase 3
Recruiting
Conditions
ST Elevation myocardial infarction.
ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction
Registration Number
IRCT20220809055645N7
Lead Sponsor
Rasht University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
54
Inclusion Criteria

Patients with ST segment elevation myocardial infarction (STEMI) undergoing successful Primary PCI without complications
Based on New York Heart Association (NYHA) functional class I,II,III
Informed consent for participation in study

Exclusion Criteria

Failure of primary PCI
Empagliflozin contraindications
Valvular heart disease with moderate and higher severity
Patients who need hemodynamic support during hospitalization
Not willing to continue participation in study
Receiving drugs ,eg Non-steroidal anti-inflammatory drugs (NSAIDs) which can not be denied

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Myocardial reinfarction. Timepoint: During 40-day follow up. Method of measurement: According to symptoms and ECG findings.;Stroke. Timepoint: During 40-day follow up. Method of measurement: According to symptoms and physical examinations.;Cardiac mortality. Timepoint: During 40-day follow up. Method of measurement: Cardiac death according to AHA guideline determined as paroxysmal cardiac arrest with no respiratory and circulatory response.
Secondary Outcome Measures
NameTimeMethod
Ejection fraction. Timepoint: During 40-day follow up. Method of measurement: By echocardiography.;Systolic heart failure. Timepoint: During 40-day follow up. Method of measurement: By echocardiography.;Re admission. Timepoint: During 40-day follow up. Method of measurement: Documented records.;Angina. Timepoint: During 40-day follow up. Method of measurement: History.;Second revascularization. Timepoint: During 40-day follow up. Method of measurement: Based on symptoms ECG and echocardiographic findings.;Empagliflozin complications. Timepoint: During 40-day follow up. Method of measurement: Based on history, symptoms and echocardiography findings.
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