Skip to content

Comparison of Free-breathing 3D Quantitative Perfusion in Patients With MINOCA and MINOCA-mimics

Comparison of Free-breathing 3D Quantitative Perfusion in Patients With MINOCA, Tako-Tsubo, SCAD, Myocarditis and NSTEMI in the Acute Phase and Post Convalescence

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06323811
Acronym
COPE-CMR
Enrollment
75
Registered
2024-03-21
Start date
2023-06-15
Completion date
2025-12-31
Last updated
2024-03-21

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

Conditions

Myocardial Infarction With Non-Obstructive Coronary Artery, Myocarditis Acute, Non ST Elevation Myocardial Infarction, Spontaneous Coronary Artery Dissection, Takotsubo Cardiomyopathy

Keywords

MINOCA, MINOCA-mimics, CMR, 3D perfusion, advanced CMR imaging

Brief summary

This clinical study examines patients presenting with acute myocardial infarction and no significant coronary artery disease on coronary angiography (MINOCA) and patients with MINOCA-mimics with advanced CMR. The present study aims to: * assess the microvascular function with a novel quantitative 3D myocardial perfusion imaging approach in the acute phase and post-convalescence * refine the role and diagnostic potential of advanced quantitative CMR imaging * assess the potential prognostic significance of microvascular dysfunction and epicardial adipose tissue on cardiovascular outcomes Participants will undergo advanced CMR imaging in the acute setting (within 10 days after event) and post convalescence (after 3 months).

Detailed description

Advanced CMR includes a novel free-breathing motion-informed locally low-rank quantitative 3D myocardial perfusion imaging. Perfusion imaging will be compared with 3D late gadolinium enhancement (LGE) imaging. A cine Dixon sequence is performed for the assessment of epicardial adipose tissue (EAT).

Interventions

DIAGNOSTIC_TESTCMR

Advanced CMR imaging including a novel quantitative free-breathing 3D perfusion sequence, 3D LGE imaging and a cine Dixon sequence

Sponsors

ETH Zurich
CollaboratorOTHER
University of Zurich
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Investigator)

Intervention model description

5 groups of patients (MINOCA, myocarditis, Takotsubo cardiomyopathy, SCAD, NSTEMI) will undergo CMR with 3D perfusion in the acute setting (within 10 days after the event) and post convalescence (after 3 months)

Eligibility

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

Inclusion criteria

* acute presentation with signs/symptoms of acute coronary syndrome or myocarditis * elevated cardiac biomarkers * no signficant coronary artery disease on coronary angiogram or coronary CT

Exclusion criteria

* pacemaker/other devices or claustrophobia * severe asthma, chronic obstructive lung or kidney disease * acute pulmonary embolism * arrhythmia on ECG * moderate to severe valvular disease

Design outcomes

Primary

MeasureTime frameDescription
Myocardial perfusion reserve indexwithin 10 days and after 3 months after index eventcomparison of microvascular function in the acute phase versus post convalescence

Secondary

MeasureTime frameDescription
epicardial adipose tissue (EAT)4 months (measured either at first or second CMR)the amount of epicardial adipose tissue
cardiovascular events5 yearsrate of cardiovascular death, myocardial infarction, recurrence of MINOCA, myocarditis, takotsubo cardiomyopathy, SCAD

Countries

Switzerland

Contacts

Primary ContactRobert Manka, Prof., MD
robert.manka@usz.ch+41442551251
Backup ContactVerena C Wilzeck, MD
verena.wilzeck@usz.ch

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026