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Not yet recruiting NCT06742905

Echo Acquisition Despite Geographic Separation by Replication of Human Movements (EAGER)

No phase Interventional Echocardiography

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An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Robot-guided echo, Standard echocardiogram.
Who it may be relevant to
Registry conditions: Echocardiography. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Australia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Echocardiographic Acquisition With Geographic Separation of Patients and Sonographers With Roboot Assistance (EAGER)

Overview

Echocardiography is a cornerstone of modern cardiology management, but access in rural and remote areas is limited. We have developed a robot ("Edler" named after the originator of echocardiography) which enables a sonographer to complete an examination at a distance. This study seeks to compare the images obtained by both methods, the completeness of the exam over a feasible time, and to identify particular components of the exam that are difficult to obtain using the robot.

Detailed description

The EAGER study is an effectiveness and feasibility trial of robot -assisted echo.

Patients who have undergone a standard echo will be asked to have a repeat study with a different sonographer, working remotely, obtaining images using the robot. This study is limited to 1 hour and as many views as possible will be obtained. During the study, the remote sonographer and patient are in direct contact over a video link. Another person will be in the room with the patient and the patient will be instructed on the use of a stop switch which will disengage the robot if they feel uncomfortable.

The acquired images will be saved to the imaging cloud and interpreted by an imaging specialist blinded to the original echocardiogram. A side-by-side comparison will be undertaken for each view, and image quality and study completeness will be assessed.

Interventions

  • Diagnostic test Robot-guided echo
    This echo will be performed by a remote sonographer, though a robot
  • Diagnostic test Standard echocardiogram
    Echocardiogram acquired by a sonographer at the patient's bedside

Primary outcome measures

  • Proportion complete [Time frame: 1 hour]
Secondary outcome measures (2)
  • Proportion complete [Time frame: 1 hour]
  • Proportion diagnostic features correctly identified by robotic echo [Time frame: 1 hour]

Eligibility criteria

Inclusion criteria

  • Having a conventional echocardiogram

Exclusion criteria

  • Declined consent to undergo both examinations

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Sequential
Masking
Single blind
Primary purpose
Diagnostic

Study locations

Australia · 1 center
  • Baker Heart and Diabetes Institute — Melbourne

Identifiers

NCT: NCT06742905 · BakerHeartDiabetesI

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗