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Clinical Trials/NCT03516578
NCT03516578
Completed
Not Applicable

Comprehensive Cardiac Magnetic Resonance Imaging For Prognosis Assessment After Non-ST-Elevation Myocardial Infarction

Heart Center Leipzig - University Hospital0 sites314 target enrollmentJanuary 1, 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myocardial Infarction
Sponsor
Heart Center Leipzig - University Hospital
Enrollment
314
Primary Endpoint
Major adverse cardiac events
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The prognostic significance of cardiac magnetic resonance (CMR) derived parameters of myocardial and microvascular injury has not been fully elucidated yet in non-ST-Elevation myocardial infarction (NSTEMI) patients. In the present study the investigators aim to comprehensively investigate the prognostic significance of CMR in a prospective, multicentre registry cohort of NSTEMI patients undergoing early percutaneous coronary intervention (PCI). CMR will be performed within the first week following the index event. The primary endpoint is defined as a composite of death, reinfarction, and new congestive heart failure (major adverse cardiac events) at 12 months.

Registry
clinicaltrials.gov
Start Date
January 1, 2011
End Date
March 28, 2018
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Heart Center Leipzig - University Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients are eligible for the study if they have: 1) ischemic symptoms in accordance with a possible NSTEMI diagnosis; 2) elevated cardiac troponin levels above the 99th percentile; and 3) identifiable culprit lesion during early invasive coronary angiography with performed PCI.

Exclusion Criteria

  • STEMI; 2) presence of cardiogenic shock; 3) no identifiable culprit lesion or culprit lesion ineligible for PCI; 4) indication for acute bypass surgery; 5) age less than 18 years or more than 90 years; 6) pregnancy; and 7) typical contraindications to CMR (e.g. severe claustrophobia, implanted pacemakers and internal cardioverter defibrillators, cerebral or intracranial metallic implants, known allergy to gadolinium and creatinine clearance \<30 mL/min).

Outcomes

Primary Outcomes

Major adverse cardiac events

Time Frame: 12 months

Composite of death, reinfarction and new congestive heart failure

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