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Completed

NCT Number: NCT06903754

ISGLT2 in Patients Without DM With Acute MI

This study will evaluate the effect of ISGLT2 (Dapagliflozin or Empalgliflozin), administered once daily in addition to standard of care treatments for non-diabetic patients with myocardial infarction (MI) treated with PCI, on hospitalization for heart failure, readmissions for acute coronary syndrome and all-cause mortality.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Mohammed VI university hospital oujda

OUDA, Morocco

About this study

This is a single-center, prospective study in non-diabetic patients with acute coronary syndrome (ACS) (ST elevation (STEMI) or non-ST elevation (NSTEMI) with left ventricular systolic dysfunction (Defined as Ejection Fraction<50% assessed by 2D Simson Bi-plane echocardiography) or evidence of acute de Novo heart failure. The study will assess the effect of dapagliflozin or empagliflozin versus placebo, administered once daily in addition to standard therapy, on HF hospitalizations, all-cause deaths and ACS readmissions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participant must approved the informed consent.
  • Confirmed MI, either STEMI or NSTEMI, according to the fourth universal definition of MI (Thygesen et al 2019).
  • Evidence of impaired regional or global LV systolic function at any timepoint during current MI-related hospitalisation with Ejection Fraction<50%(established with echocardiogram, radionuclide ventriculogram, contrast angiography or cardiac MRI) or Symptoms of Acute heart failure without cardiogenic Shock.
  • Hemodynamically stable (no episodes of symptomatic hypotension, or arrhythmia with haemodynamic compromise in the last 24 hours).

Exclusion criteria

  • Known type 1 diabetes mellitus (T1DM) or T2DM at the time for admission.
  • Chronic symptomatic HF with a prior HHF within the last year and known reduced ejection fraction (LVEF≤40 %), documented before the current MI hospitalization.
  • Patients with cardiogenic shock who received vasoactive drugs during index.
  • Hospitalization Severe (eGFR <20 mL/min/1.73 m2 by local laboratory), unstable or rapidly progressing renal disease at the time of randomization
  • Severe hepatic impairment (Child-Pugh class C) at the time of inclusion into the trial.
  • Active malignancy requiring treatment at the time of screening.
  • Any non-CV condition, eg malignancy, with a life expectancy of less than one years based on the investigator´s clinical judgement.
  • Currently on treatment, or with an indication for treatment, with a sodium glucose co-transporter 2 inhibitor (SGLT2-inhibitor)

Treatment and study plan

With ISGLT2

Drug

Patients for whom we will prescribe ISGLT2

Primary outcomes

  1. Primary endpoints

    Time frame: 50 months

    Time to the first occurrence of any of the components of this composite: hospitalization for heart failure (HHF), Non fatal Myocardial infarction (MI) or Death from all causes

Secondary outcomes

  1. Secondary outcomes

    Time frame: 50 months

    Time to the first occurrence of a fatal or a non-fatal MI [Time Frame: From admission visit (Day 0) up to approximately 4.2years] Time to first hospitalisation for Heat failure [Time Frame: From admission visit (Day 0) up to approximately 3 years] Time to death of any cause [Time Frame: From admission visit (Day 0) up to approximately 4.2 years] Time to new onset of type 2 diabetes mellitus (T2DM) post discharge [Time Frame: From admission (Day 0) up to approximately 4.2 years] Time to new onset atrial fibrilation (AF) post discharge [Time Frame: From admission visit (Day 0) up to approximately 4.2 years]

Sponsors and collaborators

Lead sponsor

Mohammed VI University Hospital

Other

Registry information

Official study title

Sodium Glucose Cotransporter 2 Inhibitors in Patients Without Diabetes With Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention

Acronym: ISGTL2-MORMI

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Apr 1, 2025
Registry last updated
Sep 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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