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EMVision First Responder Brain Scanner in Aeromedical Retrievals

Workflow Assessment and Usability of the EMVision First Responder Brain Scanner in Aeromedical Retrievals

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625001153404
Enrollment
30
Registered
2025-10-21
Start date
2025-11-01
Completion date
2026-03-01
Last updated
2025-10-27

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 study is workflow assessment and usability study of the EMVision First Responder Brain Scanner in aeromedical workflows. This study collects EMVision brain scans including workflow metrics generated from scan procedures timestamps. This study hypothesises that the proposed EMVision First Responder Brain Scanner aeromedical workflow is suitable for use in an emergency aeromedical stroke response.

Interventions

This trial implements an aeromedical workflow for the EMVision First Responder Brain Scanner in fixed-wing aeromedical retrievals. This study aims to assess the aeromedical workflow with the inclusion of a EMVision First Responder Brain Scan procedure. Participants undergoing a non-emergency aeromedical retrieval will receive an EMVision First Responder brain scan. This brain scan measures the dielectric properties of the brain using non-invasive, non-ionising, low-energy, electromagnetic pulse

This trial implements an aeromedical workflow for the EMVision First Responder Brain Scanner in fixed-wing aeromedical retrievals. This study aims to assess the aeromedical workflow with the inclusion of a EMVision First Responder Brain Scan procedure. Participants undergoing a non-emergency aeromedical retrieval will receive an EMVision First Responder brain scan. This brain scan measures the dielectric properties of the brain using non-invasive, non-ionising, low-energy, electromagnetic pulses. During an EMVision First Responder brain scan procedure, the EMVision First Responder Brain Scanner is brought to a participant lying supine on a comfortable flat surface (i.e., stretcher, bed). A headset housing an array of antennae is placed on the head, where the headset membrane inflates with a coupling fluid to conform to the shape of the head during which the scans take place. Participation in this study consists of a single visit taking place at the destination of an aeromedical retrieval (i.e., not during a flight) and consists of a single brief scan procedure (typically under six minutes) conducted by a qualified physician, nurse or paramedic. Study participation is considered complete upon the conclusion of the EMVision First Responder brain scan. Personnel responsible for conducting scans will receive two hours of face-to-face training with EMVision trainers approximately one week prior to enrolment of the first participant. All scan data is reviewed by EMVision engineers to verify scanning procedures are conducted to an appropriate standard.

Sponsors

EMVision
Lead SponsorCommercial sector/Industry

Study design

Allocation
Non-randomised trial
Primary purpose
Diagnosis

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Adults >= 18 years of age. Patients receiving an aeromedical transport. Head size deemed suitable to fit the device. The use of the EMVision First Responder Brain Scanner will not delay the treatment of the patient.

Exclusion criteria

Cannot freely provide consent Contraindications to the EMVision First Responder Brain Scanner procedure. Suffering from or suspected of suffering from an acute head injury. Suffering from or suspected of suffering from an acute neurological condition. Unable to lie still for the duration of the expected scan time. Any other medical or logistical contraindication at the discretion of the aeromedical retrieval team or attending physician.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026