CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 8 enrolled
Drug / intervention
Investigational ultrasound examdevice
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.

Search/NCT05340244
NCT05340244N/ACompleted
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GE Cardiovascular Ultrasound Device Evaluation

GE Healthcare·interventional·Posted Apr 22, 2022·Updated Jan 10, 2023

In Brief

A clinical study evaluating Investigational ultrasound exam for Echocardiography. Completed, enrolled 8 participants across 1 site.

Detailed Summary

The purpose of the study is to collect user feedback on the Vivid E95 ultrasound system and probes during clinical procedures on the device's intended population in order to optimize the device.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsEchocardiography
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2023202420252026
First PostedApr 22, 2022
Enrollment StartJun 1, 2022
Primary CompletionJul 26, 2022
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 4.2 years ago

Interventions

Investigational ultrasound examdevice

Eligible subjects will be enrolled into the study and positioned for their ultrasound exam. Standard clinical practice procedures will be followed using the standard of care device at the site to complete the clinically indicated exams. After the clinically indicated exam, portions of the TTE and/or TEE exam will be repeated with the investigational ultrasound device.