Clinical trial Recruiting at 1 site Observational Ages 18 to 80

SGLT2 inhibitor effects on artery stiffness, vessel lining thickness, and heart muscle after a heart attack

Official title: The Effect of Sodium Glucose Co-trnasportert Type 2 Inhibitors on Arterial Stiffness, Endothelial Glycocalyx Thickness , Left Atrial and Left Ventricular Deformation After Acute Myocardial Infarction

Run by University of Athens · NCT07469943 · Data updated 2026-11-12

This project will see if SGLT2 inhibitors given after a heart attack improve blood vessel stiffness, the vessel's protective lining, and heart muscle function for people with type 2 diabetes or reduced heart pumping.

More Myocardial Infarction (MI) trials

Quick facts

Study typeObservational
Ages18 Years to 80 Years
SexAll
Enrollment80 (estimated)
SponsorUniversity of Athens
Academic / other
Locations1 site (Athens, Rimini1/Haidari)
StatusRecruiting
StartedJanuary 9, 2026
Main results expectedAugust 14, 2028
Study endsDecember 20, 2028
Registry record updatedMarch 13, 2026
Trial IDNCT07469943 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with ST-elevation myocardial infarction who have type 2 diabetes or an LVEF <40% and who meet safety criteria (eGFR ≥60, not pregnant, no active cancer or autoimmune disease) are ideal candidates.

Probably not a fit

Patients with eGFR <60 ml/min/1.73 m², active malignancy, autoimmune/autoinflammatory disease, severe hepatic impairment, or who are pregnant or breastfeeding are excluded and unlikely to receive benefit as studied.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study will follow people after ST-segment elevation myocardial infarction who have type 2 diabetes or a left ventricular ejection fraction below 40% to compare vascular and cardiac measures between those treated with SGLT2 inhibitors and those not treated. Investigators will record measurements of arterial stiffness, endothelial glycocalyx thickness, and myocardial deformation at baseline and during follow-up to track changes after the acute event. Key exclusions include significant chronic kidney disease (eGFR <60 ml/min/1.73 m²), active malignancy, autoimmune/autoinflammatory disorders, severe hepatic impairment, and pregnancy or breastfeeding. All study visits and measurements will be conducted at Attikon University Hospital in Athens as part of routine research follow-up.

Why it matters

Potential benefit: If positive, the findings could support using SGLT2 inhibitors to improve vascular function and limit adverse heart remodeling after myocardial infarction, potentially reducing heart failure and recurrent event risk.

How similar studies have gone: Large randomized trials have shown SGLT2 inhibitors reduce heart failure hospitalizations and cardiovascular death, but their specific effects on arterial stiffness, endothelial glycocalyx, and myocardial deformation after acute STEMI remain limited and underexplored.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* STEMI participants with type 2 diabetes or LVEF\<40%

Exclusion Criteria:

1. Chronic kidney disease with estimated glomerular filtration rate (eGFR) \<60 ml/min/1.73 m²
2. Active malignancy
3. Autoimmune or autoinflammatory disorders
4. Severe hepatic impairment
5. Pregnancy or breastfeeding

Where it's running

  • Attikon University Hospital, 2nd Department of Cardiology, National and Kapodistrina University of Athens
    Athens, Rimini1/Haidari, Greece
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.