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NCT06599229Active, not recruiting

Perfusion Abnormalities in Hypertrophic Cardiomyopathy

Myocardial Perfusion Abnormalities in Hypertrophic Cardiomyopathy

Source: ClinicalTrials.gov · Last updated 16 Apr 2026

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
13 Sept 2024
Start date
2 Jan 2025
Primary completion date
30 May 2026
Lead sponsor
University of Virginia
NCT number
NCT06599229

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 2 Jan 2025 to the primary completion date, 30 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Allergy to ultrasound enhancing agent (lipid-stabilized) or regadenoson
  • Moderate or greater reactive airways disease

Other

  • Pregnancy
  • Lactation
  • Serious AE to regadenoson
  • Hypotension
  • Serious bradycardia not addressed by pacemaker

Who the study is looking for

  • Diagnosis of hypertrophic cardiomyopathy
  • Subject being initiated on clinically-indicated cardiac myosin inhibitor therapy

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Virginia
Coordinator of this site? Confirm its status
CharlottesvilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.