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Feasibility and clinical accuracy of novel robot-assisted, remotely-performed echocardiographic examination

Feasibility and clinical accuracy of novel robot-assisted, remotely-performed echocardiographic examination

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12623000673640
Enrollment
60
Registered
2023-06-22
Start date
2022-06-27
Completion date
2023-12-29
Last updated
2023-07-04

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

Conditions

None listed

Brief summary

This research study aims to investigate and establish the feasibility, clinical accuracy of remotely-performed, robot-assisted ehocardiographic examination (echo) performed by cardiac sonographers.

Interventions

Alternative format of non-invasive diagnostic procedure - cardiac ultrasound Procedure - Utilisation of existing clinically used cardiac ultrasound systems where system probe is held by robotic arm. Sonographer utilises a gamepad to control the robotic arm system to acquire images. Any ultrasound system is permitted, and a specific vendor is utilised based on the discretion of the hospital. Sonographers will undergo a minimum of 15 hrs of virtual (software-based only) and hand-on simulator t

Alternative format of non-invasive diagnostic procedure - cardiac ultrasound Procedure - Utilisation of existing clinically used cardiac ultrasound systems where system probe is held by robotic arm. Sonographer utilises a gamepad to control the robotic arm system to acquire images. Any ultrasound system is permitted, and a specific vendor is utilised based on the discretion of the hospital. Sonographers will undergo a minimum of 15 hrs of virtual (software-based only) and hand-on simulator training, prior to human scanning. Standard operation manuals are provided to ensure correct and standardised use of the system. All participants will receive both procedures immediately after each other (consenting staff participants), or within 72hrs of each other (consenting patient participants); with the robotic arm used first and the manual probe used second (consenting staff participants), or the robotic arm used second after manual probe examination (performed for clinical purposes; sonographer blinded to the clinical exam)

Sponsors

RMI Oceania Pty Ltd
Lead SponsorCommercial sector/Industry

Study design

Allocation
Non-randomised trial
Intervention model
Other
Primary purpose
Diagnosis
Masking
Blinded (masking used) (Caregiver, Investigator)

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

equal to and greater than 18yrs old, willing and able to participate

Exclusion criteria

under 18yrs old, unwilling and/or unable to participate, known current cardiac disease or condition

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026