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Data Collection Study of the EMVision emu™ Brain Scanner of Patients Not Experiencing Stroke for Software Algorithm Development Purposes

Data Collection Study of the EMVision emu™ Brain Scanner of Patients Not Experiencing Stroke for Software Algorithm Development Purposes

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12624001476527
Enrollment
8
Registered
2024-12-18
Start date
2024-12-18
Completion date
2026-10-16
Last updated
2025-09-08

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 a data collection study of the EMVision emu™ brain scanner for patients not suffering from or suspected of suffering from an acute stroke for software algorithm development. This study collects EMVision brain scans and MRI scans from patients receiving a head MRI as part of their routine care. Scans are anonymised and enter the EMVision database for training and developing software algorithms. This study hypothesises that an expanded non-stroke dataset can improve the diagnostic performance of the emu™ brain scanner.

Interventions

This study is a data collection study for the purposes of training software algorithms. Participants who have recently received an head MRI as part of their routine care will receive two emu™ brain scans. emu™ device brain scans measure the dielectric properties of the brain using non-invasive, non-ionising, low-energy, electromagnetic pulses. During an emu™ brain scan procedure, the emu™ is brought bedside to a participant lying supine on a hospital bed. A headset housing an array of antennae

This study is a data collection study for the purposes of training software algorithms. Participants who have recently received an head MRI as part of their routine care will receive two emu™ brain scans. emu™ device brain scans measure the dielectric properties of the brain using non-invasive, non-ionising, low-energy, electromagnetic pulses. During an emu™ brain scan procedure, the emu™ is brought bedside to a participant lying supine on a hospital 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 in the hospital following the MRI brain scan. Each visit takes up to one hour and consists of two scan procedures conducted by a qualified nurse or physician, taking ten minutes each. Nurses and physicians responsible for conducting scans will receive two hours of face-to-face training or refresher training with EMVision trainers 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. Study participation is considered complete following the second emu™ brain scan; no follow-up visits or reporting is required.

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

Ability to freely provide informed consent, able to speak English, and read written English. Head size deemed suitable for scanning with the emu™ brain scanner. Completed an MRI of the head (including both T1 and T2 sequences), where the MRI identified no significant abnormalities, within the last 24 hours. Participation in the research study will not delay the treatment of the participant.

Exclusion criteria

Pregnant or breastfeeding. Known presence of medical implantation in the head. Known neck conditions/injuries. Neurological condition that presents with significant abnormalities in an MRI of the head.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026