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Comparitive Effectiveness of PME Versus Transthoracic Echocardiogram (TTE)

Comparative Effectiveness of Pocket, Mobile, Hand-held Echocardiography and Conventional Transthoracic Echocardiography in an Inpatient and Outpatient Clinical Setting

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02141269
Enrollment
200
Registered
2014-05-19
Start date
2012-06-30
Completion date
2015-05-31
Last updated
2015-05-20

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

Conditions

Cardiac Disease

Keywords

Transthoracic echocardiogram, Hand-held Echocardiography

Brief summary

A new hand held pocket echo device (GE Vscan) has now become available to clinicians, with limited data available comparing the effectiveness of this device as a screening tool when compared to traditional transthoracic echocardiography (TTE). 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.

Detailed description

A new hand held pocket echo device (GE Vscan) has now become available to clinicians, with limited data available comparing the effectiveness of this device as a screening tool when compared to TTE. 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.

Interventions

None listed

Sponsors

Scripps Translational Science Institute
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

1. All subjects with an order for a routine transthoracic echocardiogram based on clinical indications. 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

1. Subjects who had a limited transthoracic echocardiography (i.e limited views) 2. Vscan imaging not attempted for a certain parameter

Design outcomes

Primary

MeasureTime frameDescription
Comparison of HHE and TTE results1 timeComparison of the two modalities includes accuracy, sensitivity, specificity, proportion visualized, and inter-observer variability.

Countries

United States

Outcome results

None listed

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