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Assessment of Wall Thickness in Hypertrophic Cardiomyopathy

Assessment of Wall Thickness in Hypertrophic Cardiomyopathy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02234336
Enrollment
110
Registered
2014-09-09
Start date
2014-10-31
Completion date
2017-07-25
Last updated
2019-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertrophic Cardiomyopathy

Keywords

Echocardiography, hypertrophic cardiomyopathy, cardiomyopathy, magnetic resonance imaging, contrast

Brief summary

Assessment of wall thickness in hypertrophic cardiomyopathy (HCM) is of diagnostic and prognostic importance given its known association with sudden cardiac death. However, data regarding comparison of imaging modalities for this key measurement is lacking. This study seeks to compare assessment of maximum wall thickness between clinically indicated echocardiography (with and without contrast) and clinically indicated cardiac magnetic resonance imaging.

Detailed description

Patients receiving clinically indicated echocardiograms and cardiac magnetic resonance imaging at Mayo Clinic will be eligible.

Interventions

PROCEDURENoncontrast echocardiography
PROCEDURECardiac magnetic resonance imaging

Sponsors

GE Healthcare
CollaboratorINDUSTRY
Mayo Clinic
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Clinically and echocardiographically defined hypertrophic cardiomyopathy. 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

1\) Insufficient image quality for determination of maximal wall thickness.

Design outcomes

Primary

MeasureTime frameDescription
Left Ventricular Wall Thicknessapproximately 1 week after enrollmentAll subjects will undergo noncontrast echocardiography, contrast echocardiography and cardiac MRI.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026