The Effect of Early Administration of Dapagliflozin in STEMI Patients With LV Systolic Dysfunction
STEMI - ST Elevation Myocardial Infarction, Left Ventricular Systolic Dysfunction
About this trial
This is an interventional treatment trial for STEMI - ST Elevation Myocardial Infarction
Eligibility Criteria
Inclusion Criteria:
- 1st time STEMI within 24 hours undergoing PPCI. (Chest pain > 30 minutes and ST segment elevation in more than one lead, include the definition of MI with a reference: Third universal definition of MI. (published at ESC Clinical Practice Guidelines 2012).
- LVEF less than 50%.
- eGFR ≥20 mL/min/1.73 m2.
Exclusion Criteria:
- Patients less than 18 years old.
- T1D (Type I diabetes mellitus).
- Hemodynamically unstable.
- Cardiogenic shock (clinical syndrome of tissue hypoperfusion resulting from cardiac dysfunction).
- History of chronic symptomatic HF with a prior hHF within last year
- Patients on dialysis.
- Serious hypersensitivity to dapagliflozin (eg, anaphylaxis, angioedema).
- Pregnant or lactating women.
- Sever hepatic impairment.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
dapagliflozin
conventional therapy
(a) Dapagliflozin 10 mg once daily within 24 hours after PPCI for 3 month
Reperfusion therapy: primary percutaneous coronary intervention (PPCI) after DAPT loading (aspirin 300 mg and either clopidogrel 600mg or ticagrelor 180 mg orally) in the ambulance or emergency department upon diagnosis. Anti-ischemic treatment: DAPT, SC-anticoagulation, beta blockers, statin or others will be individualized according to the patient condition. Anti-failure treatment: Angiotensin converting enzyme inhibitors or angiotensin II receptor blockers, beta blockers, mineralocorticoid receptor antagonists, other diuretics will be added in case of volume overload.