University of Virginia
Charlottesville, Virginia, 22903, United States
NCT Number: NCT06599229
The purpose of this study is to investigate whether myocardial microvascular perfusion in patients with hypertrophic cardiomyopathy improved after initiation of cardiac myosin inhibitor therapy.
This study is active but is not currently recruiting participants.
18 year and older
All sexes
Observational
Charlottesville, Virginia, 22903, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Vasodilator stress myocardial contrast echocardiography will be performed at baseline and within 4 months of reaching target dose of a cardiac myosin inhibitor.
Time frame: 3 months
Myocardial contrast echo-derived myocardial blood flow at peak hyperemia (produced by regadenoson)
Time frame: 3 months
Resting myocardial perfusion by MCE
University of Virginia
Other
Myocardial Perfusion Abnormalities in Hypertrophic Cardiomyopathy
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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