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mTBI Identification and Monitoring Through Retinal Scanning

NCT06142435

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

Rebion has developed a device, the Rebion trauma tool (referred to as the head and intraocular trauma tool, or "HITT"), that detects ocular fixation and alignment using a binocular retinal scan. Preliminary data obtained from hospitalized patients with a clinically-confirmed traumatic brain injury (TBI) and uninjured controls indicates that the device can detect changes in ocular fixation, alignment, and saccades that are related to brain injury. This study seeks to evaluate the ability of the Rebion trauma tool to assess perturbations in eye movements resulting from TBI.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Brain Injuries, Traumatic

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
18 to 45 years
Sex
All
Healthy volunteers
Accepted
Sponsor
Rebiscan, Inc.
Last updated on ClinicalTrials.gov
May 20, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Massachusetts · 1

  • Boston Medical Center Concussion Clinic, Ryan Center for Sports Medicine & Rehabilitation at Boston University · Boston, MA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.