NCT06599229
Active, not recruiting
Not Applicable
Myocardial Perfusion Abnormalities in Hypertrophic Cardiomyopathy
ConditionsHypertrophic Cardiomyopathy (HCM)
Interventionsmyocardial contrast echo
Overview
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- University of Virginia
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Peak hyperemic perfusion
Overview
Brief Summary
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.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Diagnosis of hypertrophic cardiomyopathy
- •Subject being initiated on clinically-indicated cardiac myosin inhibitor therapy
Exclusion Criteria
- •Pregnancy
- •Lactation
- •Allergy to ultrasound enhancing agent (lipid-stabilized) or regadenoson
- •Serious AE to regadenoson
- •Hypotension
- •Serious bradycardia not addressed by pacemaker
- •Moderate or greater reactive airways disease
Arms & Interventions
Patients with HCM initiated on cardiac myosin inhibitor therapy
Patients with HCM who are being initiated on cardiac myosin inhibitor therapy for clinically indicated reasons.
Intervention: myocardial contrast echo (Diagnostic Test)
Outcomes
Primary Outcomes
Peak hyperemic perfusion
Time Frame: 3 months
Myocardial contrast echo-derived myocardial blood flow at peak hyperemia (produced by regadenoson)
Secondary Outcomes
- Resting myocardial perfusion(3 months)
Investigators
Jonathan Lindner, MD
Professor of Medicine
University of Virginia
Study Sites (1)
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