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The aim of this study is to assess the diagnostic accuracy of CMR feature-tracking (FT) at rest & during stress with low dose dobutamine (LDD) in the evaluation of viability in ischemic cardiomyopathy (ICM) patients and compare it with delayed gadolinium enhancement (DGE).
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Exclusion criteria
All patients with a contraindication to MR study:
Patients diagnosed with recent acute coronary syndrome within 4 weeks.
Patients who had contraindications for MRI or contrast agents, and those with poor image quality due to either inadequate breath holding or arrhythmias
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Central trial contact
Abdulrahman Hamdan
Data sourced from clinicaltrials.gov
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