Multi-Center, Prospective, Consecutive, Paired Diagnosis, Diagnostic Performance Study of the EMVision Emu™ Brain Scanner in the Detection of Intracranial Hemorrhage in Suspected Stroke Patients

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

The purpose of this research is to evaluate a new investigational device for the diagnosis of stroke, the EMVision emu™ Brain Scanner. Stroke is the result of a blood clot stopping the normal flow of blood in the brain (ischaemic stroke) or a breakage in a blood vessel causing bleeding in the brain (haemorrhagic stroke). Stroke is a medical emergency and must be quickly diagnosed and treated. Computed tomography (CT) or magnetic resonance imaging (MRI) scans are commonly used to diagnose stroke, but they are not always readily available. EMVision has developed the emu™ Brain Scanner, a helmet-like device which scans the head using ultra-high frequency radio signals. It is portable and easy to use, making it more accessible than CT or MRI machines. Easier access to the EMVision emu™ Brain Scanner may reduce the time taken to diagnose stroke, leading to faster treatment and better health outcomes. It is the purpose of this study in the first instance to determine the accuracy of the EMVision emu™ Brain Scanner in the detection of haemorrhagic stroke.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 22
Healthy Volunteers: f
View:

• Adults ≥22 years of age

• Presenting to hospital with acute neurological deficit suspected to be stroke and within 12 hours of symptom onset

• The use of the EMVision emu™ Brain Scanner will not delay the treatment of the patient

• CT or MRI brain imaging following clinical evaluation in Emergency Department per standard of care

• Head size deemed suitable for scanning with the EMVision emu™ Brain Scanner -

Locations
United States
Florida
Mayo Jacksonville
NOT_YET_RECRUITING
Jacksonville
Texas
UTHealth
NOT_YET_RECRUITING
Houston
Other Locations
Australia
Liverpool Hospital
NOT_YET_RECRUITING
Liverpool
Royal Melbourne Hospital
RECRUITING
Parkville
Contact Information
Primary
Christian Wight, PhD
cwight@emvision.com.au
61 (0) 490 109 797
Backup
Sadie Burnham
sburnham@vastrax.com
7742078910
Time Frame
Start Date: 2025-03-26
Estimated Completion Date: 2026-11-28
Participants
Target number of participants: 300
Treatments
Intracranial Haemorrhage Group A
Other Group B
Group B includes all patients enrolled in the study ultimately diagnosed with a condition other than intracranial haemorrhage, including ischaemic stroke, transient ischaemic attack, or any of a variety of stroke mimicking conditions.
Related Therapeutic Areas
Sponsors
Leads: EMVision Medical Devices Ltd

This content was sourced from clinicaltrials.gov