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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01197677
Other study ID # Euro CMR
Secondary ID
Status Completed
Phase N/A
First received September 7, 2010
Last updated September 5, 2016
Start date April 2009
Est. completion date October 2013

Study information

Verified date September 2016
Source Stiftung Institut fuer Herzinfarktforschung
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Observational

Clinical Trial 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 have a completely normal CMR scan will have a low risk for cardiovascular events.

2. The main aim of the second specific protocol initiated by the European CMR registry, HCM-SCD, will be to evaluate CMR for risk stratification in hypertrophic cardiomyopathy(HCM).

3. This registry is sought to collect data on the general use of CMR in the European clinical practice, its safety and its therapeutic implications in a high number of cases to 1) substantiate the clinical yield of CMR and 2) to define additional clinical questions worth to be investigated in detail as additional specific protocols in the future.


Recruitment information / eligibility

Status Completed
Enrollment 30000
Est. completion date October 2013
Est. primary completion date September 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 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 Criteria:

- 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)

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Consecutive Patients Undergoing CMR

Locations

Country Name City State
Germany Klinikum Coburg Coburg
Germany Elisabeth Krankenhaus Essen
Germany Cardioangiologisches Centrum Bethanien Frankfurt
Germany Krankenhaus Agatharied Hausham
Germany Klinikum Ludwigsburg-Bietigheim Ludwigsburg
Germany Robert Bosch Medical Centre Stuttgart
Germany Klinikum Traunstein Traunstein
Italy Clinical Physiology Institute Pisa
Spain Hospital de la Santa Creu i Sant Pau Barcelona
Switzerland Centre Hospitalier Universitaire Vaudois Lausanne

Sponsors (1)

Lead Sponsor Collaborator
Stiftung Institut fuer Herzinfarktforschung

Countries where clinical trial is conducted

Germany,  Italy,  Spain,  Switzerland, 

References & Publications (3)

Bruder O, Schneider S, Nothnagel D, Dill T, Hombach V, Schulz-Menger J, Nagel E, Lombardi M, van Rossum AC, Wagner A, Schwitter J, Senges J, Sabin GV, Sechtem U, Mahrholdt H. EuroCMR (European Cardiovascular Magnetic Resonance) registry: results of the German pilot phase. J Am Coll Cardiol. 2009 Oct 6;54(15):1457-66. doi: 10.1016/j.jacc.2009.07.003. Epub 2009 Aug 13. — View Citation

Bruder O, Wagner A, Mahrholdt H. Lessons Learned from the European Cardiovascular Magnetic Resonance (EuroCMR) Registry Pilot Phase. Curr Cardiovasc Imaging Rep. 2010 Jun;3(3):171-174. Epub 2010 Apr 13. — View Citation

Wagner A, Bruder O, Schneider S, Nothnagel D, Buser P, Pons-Lado G, Dill T, Hombach V, Lombardi M, van Rossum AC, Schwitter J, Senges J, Sabin GV, Sechtem U, Mahrholdt H, Nagel E. Current variables, definitions and endpoints of the European cardiovascular magnetic resonance registry. J Cardiovasc Magn Reson. 2009 Nov 5;11:43. doi: 10.1186/1532-429X-11-43. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary collect data from a large number of patients regarding the general use of CMR in European clinical practice, its safety and its therapeutic implications 01/01/2009- No
Secondary to show that a normal CMR protocol (incl. LV wall motion at rest, stress ischemia, and scar detection) predicts a low risk of future cardiovascular events. 01/01/2009 No
Secondary to evaluate if myocardial scarring assessed by contrast-enhanced CMR is a stronger predictor of adverse events during follow up than the general clinical markers of an adverse long term outcome in HCM. 01/01/2009- No

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