Effect of Mavacamten Treatment on Coronary Flow Reserve in oHCM
Part of paid clinical trials in Charlottesville, Virginia.
- Sponsor
- Michael Ayers
- Study ID
- NCT06023186
- Status
- Recruiting
Conditions
- Obstructive Hypertrophic Cardiomyopathy
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 85 Years
- Healthy Volunteers
- Not accepted
Interventions
- mavacamten — DRUGStudy participants will receive mavacamten under the standard of care
Study Details
The goal of this observational study is to measure the effect of mavacamten treatment on blood flow in the heart muscle (myocardium) in patients with obstructive hypertrophic cardiomyopathy. The main question it aims to answer is: • Does mavacamten treatment improve blood flow in the heart muscle? Participants will take mavacamten at the direction of their treating physician. Participants will complete 2 myocardial Positron Emission Tomography and Computed Tomography (PET-CT) scans. The first scan will be completed before participants start taking mavacamten. The scan will be repeated after 12 months of mavacamten treatment.
Key Dates
- Start date
- Nov 3, 2023
- Status verified
- Nov 2024
- Primary completion
- Aug 31, 2026
- Completion
- Sep 30, 2026
Study Design
- Enrollment
- 20 participants (estimated)
Arms
- Arm: Cohort 1Clinically stable, adult patients with obstructive hypertrophic cardiomyopathy, who meet mavacamten prescribing guidelines will be prescribed mavacamten by their treating physician.
Primary Outcome Measure
Change in myocardial perfusion reserve after 12 months of mavacamten treatment. [ Time Frame: 12 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Virginia | Charlottesville | Virginia | 22908 | Michael Ayers, MD (PRINCIPAL_INVESTIGATOR) |
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