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Clinical Trials/NCT00529607
NCT00529607
Completed
Not Applicable

New Imaging and Diagnostic Techniques for the Assessment of Reperfusion Injury in Myocardial Infarction.

RWTH Aachen University1 site in 1 country200 target enrollmentSeptember 2007

Overview

Phase
Not Applicable
Intervention
contrast echocardiography
Conditions
Reperfusion Injury
Sponsor
RWTH Aachen University
Enrollment
200
Locations
1
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

The primary purpose of this study is to correlate new cardiac imaging modalities (2D, 3D echocardiography, contrast echocardiography, strain analysis and cardiac MRI) to biochemical parameters as the L-arginine-nitric oxide pathway and inflammatory cascades to characterize the reperfusion injury following myocardial infarction and thus providing a basis for further diagnostic and therapeutic approaches.

Detailed Description

By reperfusion of ischemic myocardium further tissue damage occurs (ischemia / reperfusion injury). Various contributing mechanisms have been discussed in experimental studies, e.g. disturbances in coronary microcirculation and consecutive induction of inflammatory cascades involving formation of reactive oxygen species. The ischemia / reperfusion injury causes diastolic and regional as well as global systolic dysfunction. The time course of the reperfusion injury within the first hours after reperfusion and its effects on the global geometry of the left ventricle have not been investigated so far. In the present study a comprehensive morphological and functional characterisation of the ischemia / reperfusion injury in the acute phase is performed. New cardiac imaging modalities (2D, 3D echocardiography, contrast echocardiography, strain analysis and cardiac MRI)and biochemical parameters including the L-arginine-nitric oxide pathway and inflammatory cascades are applied. Hereby morphological and biochemical markers for the functional recovery of myocardial function should be identified.

Registry
clinicaltrials.gov
Start Date
September 2007
End Date
March 2009
Last Updated
17 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • patients with acute ST elevation myocardial infarction and consecutive percutaneous coronary intervention of the infarct-related artery (first myocardial infarction and recurrent myocardial infarction, as long as infarct-related artery is occluded for the first time)
  • written informed consent
  • or 30 patients with stable CAD (control group 1) or 30 healthy volunteers regarding cardiovascular diseases (control group 2)

Exclusion Criteria

  • incompetent persons
  • pregnant and lactating
  • moderate to severe renal insufficiency defined by an GFR \< 60 ml/kg/m2
  • missing written consent
  • other reasons complicating a clinical reevaluation and/or coronary angiography

Arms & Interventions

1

- patients with acute ST elevation myocardial infarction and consecutive percutaneous coronary intervention of the infarct-related artery

Intervention: contrast echocardiography

1

- patients with acute ST elevation myocardial infarction and consecutive percutaneous coronary intervention of the infarct-related artery

Intervention: 2D and 3D echocardiography

1

- patients with acute ST elevation myocardial infarction and consecutive percutaneous coronary intervention of the infarct-related artery

Intervention: cardiac MRI

1

- patients with acute ST elevation myocardial infarction and consecutive percutaneous coronary intervention of the infarct-related artery

Intervention: blood sampling

2

- 30 patients with stable CAD (control group 1)

Intervention: blood sampling

3

- 30 healthy volunteers regarding cardiovascular diseases (control group 2)

Intervention: blood sampling

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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