Comparitive Effectiveness of PME Versus Transthoracic Echocardiogram (TTE)
NCT ID: NCT02141269
Last Updated: 2015-05-20
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
200 participants
OBSERVATIONAL
2012-06-30
2015-05-31
Brief Summary
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The investigators are evaluating the effectiveness of this hand-held echo (HHE) device in detecting cardiac pathology in a both an inpatient and outpatient clinical setting as compared to a comprehensive TTE evaluation.
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Detailed Description
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We are evaluating the effectiveness of this HHE device in detecting cardiac pathology in a both an inpatient and outpatient clinical setting as compared to a comprehensive TTE evaluation.
This study compares the images from the two modalities with regards to multiple parameters typically evaluated by traditional TTE. This would include the following:
1. Ejection fraction: estimates how well the heart is squeezing/functioning.
2. Segmental wall motion abnormalities: if one wall of the heart is not moving well, this suggests that part of the heart is not getting enough blood supply and could represent a blockage in a blood vessel supplying the heart or in other terms a heart attack.
3. Left ventricular end-diastolic dimension: allows us to see if the heart is dilated
4. Inferior vena cava size: the size of this great vein can help estimate if patient has too much fluid in their vascular bed.
5. Aortic valve pathology: whether or not there is thickening of the valve or impairment of it's opening.
6. Mitral valve pathology: whether or not the valve is significantly thickened or with impaired closing and opening.
7. Pericardial effusion: excessive fluid in the sack around the heart.
The images obtained on the HHE will be evaluated by two experienced echocardiographers as well as two cardiology fellows who have obtained training in image acquisition and interpretation. The readers of the HHE images are blinded to the TTE results, and vice versa.
A comparison of these individual parameters on HHE and TTE allows us to validate this new, convenient screening tool in detecting cardiac pathology.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
2. Vscan images will be obtained to evaluate multiple parameters (noted on research summary).
3. Immediately after Vscan imaging, a complete transthoracic echocardiogram will be performed.
4. Images will be compared between the Vscan device and the traditional transthoracic echocardiogram.
Exclusion Criteria
2. Vscan imaging not attempted for a certain parameter
18 Years
ALL
Yes
Sponsors
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Scripps Translational Science Institute
OTHER
Responsible Party
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Eric Topol, MD
Principal Investigator
Principal Investigators
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Eric Topol, MD
Role: PRINCIPAL_INVESTIGATOR
Scripps Health
Locations
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Scripps Green Hospital
La Jolla, California, United States
Countries
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Other Identifiers
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12-5906
Identifier Type: -
Identifier Source: org_study_id
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