Clinical Trials Directory

Trials / Unknown

UnknownNCT02560467

Perfusion Imaging With Myocardial Contrast Echocardiography in HCM

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Oregon Health and Science University · Academic / Other
Sex
All
Age
19 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to determine whether myocardial contrast echocardiography in patients with cardiomyopathy (HCM) can detect resting hypo-perfusion due to fibrosis or stress induced perfusion defects due to associated abnormalities in intramyocardial arteries and the microcirculation. A secondary aim will be to determine whether abnormalities in perfusion are associated with either severity of symptoms (chest pain and dyspnea), presence of arrhythmias, and regional function of the septum.

Conditions

Interventions

TypeNameDescription
DRUGEcho and myocardial contrast echocardiography perfusion imagingMyocardial blood flow will be assessed by myocardial contrast echo. Perfusion at rest and stress will be quantified and compared to patient sx, degree of dysfunction on echo strain imaging, and degree of fibrosis on magnetic resonance imaging (when available) that was ordered as part of routine clinical care. Myocardial contrast echocardiography will be performed by intravenous administration of ultrasound contrast agent (Definity or Lumason) using FDA-approved dose limits. Vasodilator stress during MCE imaging will be performed using regadenoson at FDA-approved doses.

Timeline

Start date
2015-12-01
Primary completion
2019-09-01
Completion
2019-09-15
First posted
2015-09-25
Last updated
2019-06-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02560467. Inclusion in this directory is not an endorsement.