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Magnetic Resonance Imaging In Acute ST-Elevation Myocardial Infarction

Clinical Relevance of Magnetic Resonance Imaging in Acute ST-Elevation Myocardial Infarction

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04113356
Acronym
MARINA-STEMI
Enrollment
1500
Registered
2019-10-02
Start date
2011-01-31
Completion date
2031-06-30
Last updated
2021-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute ST-Elevation Myocardial Infarction

Brief summary

Cardiovascular magnetic resonance imaging enables comprehensive assessment of cardiovascular function, morphology and pathology. The investigators aim to evaluate the nature and clinical significance of magnetic resonance imaging parameters in patients presenting with first acute ST-elevation myocardial infarction.

Interventions

Cardiovascular magnetic resonance imaging will be performed within the first week after ST-elevation myocardial infarction and in a defined subgroup 4 months, 12 months and 10 years thereafter.

Sponsors

Medical University Innsbruck
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* First ST-elevation myocardial infarction according to the European Society of Cardiology/American College of Cardiology committee criteria * Primary percutaneous coronary intervention within 24 hours after symptom onset

Exclusion criteria

* Age \< 18 years * Any history of a previous myocardial infarction or coronary intervention * Clinically unstable patients (Killip class \>2) * Renal failure (estimated glomerular filtration rate \< 30 ml/min/1.73 m2) * Contraindications to cardiac magnetic resonance imaging (pacemaker, cerebral aneurysm clip, orbital foreign body, known or suggested contrast allergy to gadolinium, claustrophobia) * Inability to provide informed consent

Design outcomes

Primary

MeasureTime frame
Occurence of major adverse cardiovascular events1 - 5 years

Secondary

MeasureTime frameDescription
Assessment of infarct transmurality grade (%) with late gadolinium enhancement imagingbaseline, 4 months and 12 months
Occurence and area of microvascular obstructionbaseline
Intramyocardial haemorrhage assessed by T2* imagingbaseline, 4 months and 12 months
Tissue characterisation by T1, T2 and T2* Mappingbaseline, 4 months and 12 months
Myocardial deformation by strain analysisbaseline, 4 months and 12 months
Chamber volumes by cine imagingbaseline, 4 months and 12 months
Cardiac function by cine imagingbaseline, 4 months and 12 months
Infarct size assessment (% of left ventricular myocardial mass)baseline, 4 months and 12 months
Aortic pulse wave velocity and distensibility by phase contrast imagingbaseline, 4 months and 12 months
Aortic pulse wave distensibility by phase contrast imagingbaseline, 4 months and 12 months
Quality of life and invalidity assessment (Global Physical Activity Questionnaire)1 - 5 years
Biomarker release during the acute and subacute phasebaseline, 4 months and 12 monthsbiomarker concentrations of hemodynamic stress (n-terminal pro-B-type natriuretic peptide), neurohumoral markers (i.e. neprilysin ng/ml), inflammatory markers (i.e. procalcitonin µg/l) and markers of myocardial injury (i.e. high sensitivity cardiac troponin T ng/l)
Parameters of cardiac function by transthoracic echocardiographybaseline, 4 months and 12 months
Plaque volume by 3D ultrasoundbaseline, 12 months
Cardiac autonomic functionbaseline, 4 months and 12 monthsDeceleration capacity of heart rate
Stroke volumes by phase contrast imagingbaseline, 4 months and 12 months

Countries

Austria

Contacts

Primary ContactBernhard Metzler, MD, MSc
bernhard.metzler@tirol-kliniken.at
Backup ContactGert Klug, MD
gert.klug@tirol-kliniken.at

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026