Myocardial Blood Volume Measurement by Real-Time Myocardial Perfusion Echocardiography Correlates to Myocardial Compressibility by Cardiac Magnetic Resonance Imaging in Healthy Subjects
NCT ID: NCT04724304
Last Updated: 2022-04-07
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
NA
115 participants
INTERVENTIONAL
2021-02-09
2021-11-11
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
SCREENING
NONE
Study Groups
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Healthy adults
Healthy adults will have blood flow to the heart evaluated using s Real-Time Myocardial Echocardiography (RTMPE) and magnetic resonance image (MRI) to the heart.
Real-Time Myocardial Echocardiography (RTMPE)
Uses sound waves (ultrasound) to produce an images of the heart. During RTMPE a microbubble contrast agent is administered through an intravenous line (IV) to make the images of your heart clearer.
Magnetic resonance image (MRI)
Imaging that focuses on the heart or blood vessels to assess size and function of the heart's chambers, thickness and movement of the walls of the heart, and blood flow in the blood vessels.
Interventions
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Real-Time Myocardial Echocardiography (RTMPE)
Uses sound waves (ultrasound) to produce an images of the heart. During RTMPE a microbubble contrast agent is administered through an intravenous line (IV) to make the images of your heart clearer.
Magnetic resonance image (MRI)
Imaging that focuses on the heart or blood vessels to assess size and function of the heart's chambers, thickness and movement of the walls of the heart, and blood flow in the blood vessels.
Eligibility Criteria
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Inclusion Criteria
* Available for testing performed in Rochester, MN.
* Willing to undergo both an echocardiogram with RTMPE and CMR.
* Study subject providing consent.
Exclusion Criteria
* BMI \<30 kg/m\^2.
* Hypertension.
* Diabetes Mellitus.
* Stroke.
* Cardiomyopathy or structural heart disease.
* Known coronary artery disease or history of myocardial infarction.
* Contraindication to echo enhancement agent or gadolinium administration such as an allergy.
* Renal GFR \< 50 mL/mL.
* Females who are pregnant.
* Subject unwilling to consent.
18 Years
ALL
Yes
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Courtney E. Bennett
Principal Investigator
Principal Investigators
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Courtney Bennett, D.O.
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo clinic Rochester
Rochester, Minnesota, United States
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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20-000936
Identifier Type: -
Identifier Source: org_study_id
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