Assessment of Wall Thickness in Hypertrophic Cardiomyopathy

NCT ID: NCT02234336

Last Updated: 2019-02-05

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

110 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-10-31

Study Completion Date

2017-07-25

Brief Summary

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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

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

Conditions

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Hypertrophic Cardiomyopathy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Subjects with HCM

All subjects will undergo noncontrast echocardiography, contrast echocardiography and cardiac MRI.

Noncontrast echocardiography

Intervention Type PROCEDURE

Contrast Echocardiography

Intervention Type PROCEDURE

Cardiac magnetic resonance imaging

Intervention Type PROCEDURE

Interventions

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Noncontrast echocardiography

Intervention Type PROCEDURE

Contrast Echocardiography

Intervention Type PROCEDURE

Cardiac magnetic resonance imaging

Intervention Type PROCEDURE

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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GE Healthcare

INDUSTRY

Sponsor Role collaborator

Mayo Clinic

OTHER

Sponsor Role lead

Responsible Party

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Patricia A. Pellikka

Professor of Medicine, College of Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

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

Site Status

Countries

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United States

Other Identifiers

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14-004757

Identifier Type: -

Identifier Source: org_study_id

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