Assessment of Wall Thickness in Hypertrophic Cardiomyopathy
NCT ID: NCT02234336
Last Updated: 2019-02-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
110 participants
OBSERVATIONAL
2014-10-31
2017-07-25
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Subjects with HCM
All subjects will undergo noncontrast echocardiography, contrast echocardiography and cardiac MRI.
Noncontrast echocardiography
Contrast Echocardiography
Cardiac magnetic resonance imaging
Interventions
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Noncontrast echocardiography
Contrast Echocardiography
Cardiac magnetic resonance imaging
Eligibility Criteria
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Inclusion Criteria
2. Clinically indicated transthoracic echocardiography as part of the medical evaluation.
3. No contradiction to administration of ultrasonic echocardiography contrast.
4. Planned clinically indicated cardiac magnetic resonance imaging as part of medical evaluation.
5. No contraindication to cardiac magnetic resonance imaging (such as cochlear implants, central nervous system aneurysm clips and other implanted medical devices).
6. Age 18 years and older
Exclusion Criteria
18 Years
ALL
No
Sponsors
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GE Healthcare
INDUSTRY
Mayo Clinic
OTHER
Responsible Party
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Patricia A. Pellikka
Professor of Medicine, College of Medicine
Principal Investigators
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Patricia Pellikka, MD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Other Identifiers
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14-004757
Identifier Type: -
Identifier Source: org_study_id
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