Diagnostic Study of the EMVision Emu™ Brain Scanner for Stroke

This study is evaluating a new device called the EMVision emu™ Brain Scanner. This scanner uses radio waves to look for bleeding in the brain (hemorrhagic stroke) in people who might be having a stroke. Strokes happen when blood flow to the brain is interrupted, either by a clot or bleeding, and quick diagnosis is very important. Currently, CT or MRI scans are used, but they aren't always available. The emu™ Brain Scanner is a portable, helmet-like device that aims to be more accessible. Researchers want to see if the emu™ Brain Scanner can detect bleeding in the brain with over 80% accuracy compared to standard CT or MRI scans. You may be able to join if you are an adult aged 22 or older, suspected of having a stroke within 24 hours of symptoms, and your head fits the scanner. The study is currently recruiting 300 participants.

Study design
This is an observational study comparing the EMVision emu™ Brain Scanner's results to standard CT or MRI scans in 300 participants. It is not specified if it is blinded or randomized.
What's involved
You would receive a scan with the EMVision emu™ Brain Scanner. This happens alongside your usual stroke care, so it won't delay your treatment. You will also have standard CT or MRI brain imaging.
Compensation
Not stated in the trial record.
Follow-up
The primary goal is to measure the scanner's accuracy within 30 minutes of a standard CT/MRI. No further follow-up is specified.

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NCT06999122

Diagnostic Performance Study of the EMVision Emu™ Brain Scanner in the Detection of Intracranial Hemorrhage in Suspected Stroke Patients

Recruiting
Not specifiedAges 22+Observational
EMVision Medical Devices Ltd
~300 participants
Updated 2026-07-27 on ClinicalTrials.gov
What's tested:Brain Scan

At a glance

Recruiting sites
8 of 8 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Demonstrate haemorrhage detection sensitivity >80% and specificity >80%
Measured over <30 minutes from acute baseline CT/MRI
Stroke
Hemorrhagic Stroke

NCT06999122

Where you'd take part

This study runs at 8 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Liverpool Hospital

    Liverpool, New South Wales, Australiastudy coordinator listed

    Recruiting

  • Mayo Jacksonville

    Jacksonville, Floridastudy coordinator listed

    Recruiting

  • Memorial Hermann Memorial City Medical Center

    Houston, Texasstudy coordinator listed

    Recruiting

  • Mount Sinai Health System

    New York, New Yorkstudy coordinator listed

    Recruiting

  • Mount Sinai West

    New York, New Yorkstudy coordinator listed

    Recruiting

  • Royal Melbourne Hospital

    Parkville, Victoria, Australiastudy coordinator listed

    Recruiting

  • UCLA

    Los Angeles, Californiastudy coordinator listed

    Recruiting

  • UTHealth

    Houston, Texasstudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Reade De Leacy, MBBS(Hons) FRANZCR · PRINCIPAL_INVESTIGATOR · Associate Professor of Neurosurgery and Radiology Director of Neurointerventional Spine Site Director Cerebrovascular Services Mount Sinai Queens Co-director Neuroendovascular Surgery Fellowship Department of Neurosurgery Mount Sinai Health System
  • Angela Dos Santos, PhD · PRINCIPAL_INVESTIGATOR · Melbourne Health

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  • Demonstrate haemorrhage detection sensitivity >80% and specificity >80%<30 minutes from acute baseline CT/MRI