Overview

The Effect of Early Administration of Dapagliflozin in STEMI Patients With LV Systolic Dysfunction

Status:
Not yet recruiting
Trial end date:
2022-09-01
Target enrollment:
0
Participant gender:
All
Summary
300 STIMI patients with LV systolic dysfunction will be divided into two equal groups (Group I (Study arm, n=150); will receive dapagliflozin plus conventional therapy and group (II) Control arm (n=150); will receive conventional therapy only to detect an improvement in the LVEF by ≥ 5
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Assiut University
Treatments:
2-(3-(4-ethoxybenzyl)-4-chlorophenyl)-6-hydroxymethyltetrahydro-2H-pyran-3,4,5-triol
Adrenergic beta-Antagonists
Angiotensin II
Angiotensin Receptor Antagonists
Angiotensin-Converting Enzyme Inhibitors
Angiotensinogen
Aspirin
Clopidogrel
Dapagliflozin
Diuretics
Enzyme Inhibitors
Giapreza
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Mineralocorticoid Receptor Antagonists
Mineralocorticoids
Ticagrelor
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.