RecruitingNot ApplicableNCT06009874

Clinical Investigation of the Cardioprotective Effect of Early Administration of SGLT2 in Patients Presented With AMI

Clinical Investigation of Cardioprotective Effect of Early Administration of Sodium-glucose Cotransport-2 Inhibitors in Patients With Acute Myocardial Infarction


Sponsor

Mohammad Hussien Tantawy Soliman

Enrollment

80 participants

Start Date

Oct 1, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to investigate the effect of early administration of DAPA during ischemia and before pPCI on infarct size, reperfusion injury-related myocardial damage, cardioprotection from HF, and renoprotection from AKI in patients with AMI.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria6

  • Patients with ST-elevation myocardial infarction (STEMI).
  • STEMI was defined according to the Fourth Universal Definition of AMI.
  • 18 - 80 years of age.
  • Diabetics or non-diabetics.
  • eGFR > 45 ml/min/1.73m2.
  • Blood pressure before first drug dosing >110/70 mmHg.

Exclusion Criteria14

  • Cardiogenic shock.
  • Hypoglycemia.
  • History of diabetic ketoacidosis.
  • Genital and urinary infections.
  • History of AMI.
  • Stent thrombosis.
  • Previous coronary artery bypass surgery.
  • Severe hepatic insufficiency.
  • Advanced cancer patients.
  • Blood pH < 7.32.
  • Known allergy to SGLT-2 inhibitors.
  • Hemodynamic instability.
  • Females of childbearing potential without adequate contraceptive methods.
  • Patients currently on or have received any SGLT-2 inhibitors.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGDapagliflozin 10mg Tab

patients will be treated with DAPA 10 mg once daily for three months

DRUGPlacebo

patients will be treated with a placebo tab once daily for three months


Locations(1)

Mohammad Soliman

Shibīn al Kawm, Menofia, Egypt

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06009874


Related Trials