Status:
COMPLETED
European CMR Registry
Lead Sponsor:
Stiftung Institut fuer Herzinfarktforschung
Conditions:
Consecutive Patients Undergoing CMR
Eligibility:
All Genders
18+ years
Brief Summary
1. The main aim of the first specific protocol initiated by the European CMR registry, suspected CAD, is to demonstrate that patients presenting for work up of suspected coronary artery disease, which...
Eligibility Criteria
Inclusion
- \- European clinical practice: Consecutive patients with accomplished CMR.
- Suspected-CAD: Consecutive patients with suspected coronary artery disease undergoing a combined CMR protocol including evaluation of LV function, assessment of myocardial ische¬mia by adenosine stress perfusion or high-dose dobutamine CMR and detection of myocardial infarction using contrast-enhanced CMR.
- \- HCM-SCD: Consecutive patients with hypertrophic cardiomyopathy undergoing a combined CMR protocol including LV function, rest perfusion, and detection of myocardial scarring by contrast-enhanced CMR. The diagnosis of hypertrophic cardiomyopathy is based on the demonstration of a hypertrophied, non-dilated left ventricle (wall thickness of at least 15 mm in adults or the equivalent relative to body-surface area in children) in the absence of another cardiac or systemic disease capable of producing a similar degree of hypertrophy. In adult relatives of the patients with hypertrophic cardiomyo¬pathy, a wall thickness of 13 mm or more will be considered a criterion for diagnosis.
Exclusion
- European clinical practice: None
- Suspected-CAD: Missing informed consent. Patients with known CAD by invasive coronary angiography or previous MI.
- HCM-SCD: Missing informed consent. Patients with known CAD by invasive coronary angiography or previous MI. Patients with left ventricular hypertrophy of other causes (e.g. hypertension, valvular heart disease)
Key Trial Info
Start Date :
April 1 2009
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
October 1 2013
Estimated Enrollment :
30000 Patients enrolled
Trial Details
Trial ID
NCT01197677
Start Date
April 1 2009
End Date
October 1 2013
Last Update
September 7 2016
Active Locations (10)
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1
Klinikum Coburg
Coburg, Germany, 96450
2
Elisabeth Krankenhaus
Essen, Germany, 45138
3
Cardioangiologisches Centrum Bethanien
Frankfurt, Germany, 60389
4
Krankenhaus Agatharied
Hausham, Germany, 83734