Etiologic Mechanisms, Myocardial Changes and Prognosis of Patients With MINOCA
Myocardial Infarction With Nonobstructive Coronary Arteries
About this trial
This is an interventional other trial for Myocardial Infarction With Nonobstructive Coronary Arteries
Eligibility Criteria
Inclusion Criteria:
acute MI:
- detection of a rise and/or fall of cardiac troponin(cTn) values with at least one value above the 99th percentile upper reference limit (URL) and with at least one of the following:
- symptoms of acute myocardial ischaemia;
- new ischaemic ECG changes;
- development of pathological Q waves;
- imaging evidence of new loss of viable myocardium or new regional wall motion abnormality in a pattern consistent with an ischaemic aetiology
non-obstructive coronary arteries on angiography:
- the absence of obstructive coronary artery disease (CAD) on angiography, (i.e. no coronary artery stenosis ≥50%), in any potential infarct-related artery;
This includes both patients with:
- normal or near normal coronary arteries (no stenosis >30%)
- mild coronary atheromatosis (stenosis >30% but <50%).
- angiography performed within 24 - 48 hours
- age >18 years
- informed consent
Exclusion Criteria:
- acute kidney failure
- stage 4-5 chronic kidney disease
- contraindications for coronary angiography or CMR
- patients involved in another biomedical trial
- inability to make a decision to participate in the investigation
Sites / Locations
- Vilnius University Hospital Santaros klinikosRecruiting
Arms of the Study
Arm 1
Arm 2
Other
Other
MINOCA (group I) - conventional MI treatment
MINOCA (group II)
Traditional MI treatment with optimal doses of statin, angiotensin-converting enzyme inhibitors (ACEI) or angiotensin II receptor blockers (ARB), beta-blockers (BB) and dual antiplatelet therapy (DAPT).
Treatment with a low-dose statin and ACEI/ARB. In case of vasospasm, calcium channel blockers.