Myocardial Infarction With Nonobstructive Coronary Arteries
Conditions
Brief summary
This prospective trial will include 150 patients with myocardial infarction with non-obstructive coronary arteries (MINOCA). A thorough clinical, laboratory and imaging evaluation will be performed by novel biomarkers and modern imaging techniques (heart magnetic resonance imaging and noninvasive testing). Moreover, two different treatment groups will be distinguished. Additionally, a retrospective analysis of patients meeting MINOCA criteria will be performed.
Detailed description
Primary goals The primary trial goal is to assess the etiologic mechanisms of myocardial damage in patients with MINOCA as well as to evaluate a variety of therapeutic strategies for these patients. Secondary goals 1. To assess functional and morphological myocardial changes in patients with MINOCA; 2. To assess the true prevalence and prognostic relevance of MINOCA (all-cause mortality and MACE); 3. To test the effect of conventional acute MI therapies (BB, ACEI, ARB, CCB, statins, anti-platelet agents) on MACE (death and myocardial infarction) and all-cause mortality in patients with MINOCA; 4. To test the diagnostic and prognostic role of several biomarkers (sST2, BNP, cTnI, CRP, copeptin, procalcitonin, MR-proADM, galectin-3) in patients with MINOCA; 5. To assess the impact of MINOCA with respect to chronic health status, such as persistent angina symptoms, impairment in quality of life, and depression; 6. To evaluate systemic microcirculation status and assess its effect on long term outcomes. 7. To evaluate hospital mortality and all-cause death within 6 and 12 months follow-up; 8. To determine recurrent hospitalizations within 30-days, 6 and 12 months follow-up; 9. To assess peak creatine kinase, creatine kinase-MB and troponin levels during hospital stay; 10. To determine quality of life at 6 and 12 months assessed using the Euroqol 5D (EQ-5D) questionnaire (www.euroqol.org).
Interventions
OTHERextended clinical, laboratory and instrumental examination; treatment options comparison
Multimodality investigation and different treatment comparison
Sponsors
Research Council of Lithuania
Vilnius University Hospital Santaros Klinikos
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. 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 2. 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%). 3. angiography performed within 24 - 48 hours 4. age \>18 years 5. 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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of all-cause mortality | 12 months follow-up |
| Rate of cardiovascular death | 12 months follow-up |
Secondary
| Measure | Time frame |
|---|---|
| Rate of hospitalization for MI | 12 months follow-up |
| Rate of MACE | 12 months follow-up |
Countries
Lithuania
Contacts
Primary ContactRokas Šerpytis
Outcome results
None listed