At a glance
ClinicalIndex Comparison RecordN/ACompleted· 47 enrolled
Drug / intervention
Philips EPIQ 7 ultrasound machine +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Feasibility and Accuracy of Focused Cardiac Ultrasound Using an FDA Approved Hand-held Ultrasound Device in Outpatient Setting in Our Institution.
In Brief
A clinical study evaluating Philips EPIQ 7 ultrasound machine and Philips Lumify Broadband sector array transducer for Ventricular Dysfunction and 3 related conditions. Completed, enrolled 47 participants across 1 site.
Detailed Summary
To compare the images from standard cardiac ultrasound with images from a small hand-held device; to find out more about the feasibility and accuracy of a small hand-held ultrasound device.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2020202120222023202420252026
First PostedMar 2019
Enrollment StartApr 2019
Primary CompletionMay 2019
TodayJul 2026
First PostedMar 22, 2019
Enrollment StartApr 1, 2019
Primary CompletionMay 30, 2019
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 7.3 years ago
Interventions
Philips EPIQ 7 ultrasound machinedevice
Standard transthoracic echocardiography
Philips Lumify Broadband sector array transducerdevice
Portable hand-held ultrasound device