Coronary thrombus modification to reduce microvascular damage during STEMI care
Official title: CORonary Thrombus Modification to Prevent MIcrovascular Damage in Patients With ST-segment Elevation Myocardial Infarction (The CORMI Trial)
Run by Odense University Hospital · NCT07646977 · Data updated 2026-11-12
This study tests whether modifying the clot in the heart arteries during primary PCI can lessen microvascular damage and myocardial injury in STEMI patients.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | Odense University Hospital Academic / other |
| Locations | 1 site (Odense) |
| Status | Recruiting |
| Started | July 13, 2026 |
| Main results expected | March 2029 |
| Study ends | January 2034 |
| Registry record updated | September 2, 2026 |
| Trial ID | NCT07646977 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with STEMI planned for primary PCI and evidence of culprit coronary lesion.
✕Probably not a fit
Patients without significant microvascular dysfunction or those not undergoing primary PCI may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
In STEMI patients undergoing primary PCI, the trial explores whether altering the thrombus can reduce distal embolization and microvascular injury, with myocardial damage assessed by the myocardial salvage index at 3 months. The approach combines continuous and bolus thermodilution measurements before and after stent placement to quantify microvascular function and correlates these with cardiac MRI findings. The study also examines how invasive measurements relate to imaging biomarkers to improve understanding of microvascular dysfunction after reperfusion.
Why it matters
Potential benefit: If successful, patients may experience better restoration of microvascular flow and reduced myocardial damage after STEMI.
How similar studies have gone: Previous work suggests that thrombus modification can influence distal embolization, but this approach is relatively novel in directly reducing microvascular damage in STEMI.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * ST-elevation at the J-junction in a minimum of two contiguous ECG leads with a minimum of ≥ 0.1 mV in all leads, except for V2 and V3 (which required ≥ 0.2 for men ≥ 40 years old, ≥ 0.25 in men \< 40 years old, or ≥ 0.15 mV for all women) or new left bundle branch * Admission to hospital within 12 hours of symptom debut * Angiographic signs of a culprit lesion planned to be treated with primary percutaneous coronary intervention Exclusion Criteria: * Age \< 18 years or inability to provide informed consent * Life expectancy of \< 12 months * Hemodynamically instability * Pregnancy or breastfeeding * Known asthma or severe chronic obstructive pulmonary disease * Expected inability to perform physiological measurements (due to severely tortuous arteries, ostial disease or very distal disease), * CMR contraindications (estimated glomerular filtration rate \< 30 mL/min, magnetic or mechanically activated implants, or any prior metal implants, severe claustrophobia) * Expected to or unavoidable to use thrombectomy
Where it's running
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Odense University Hospital
Odense, Denmark Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.