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Neuro-ocular Baselines in a Sports Setting

Neuro-ocular Baselines in a Sports Setting: Feasibility Study for Head and Intraocular Trauma Test (HITT) Device for Potential Detection of Brain Dysfunction

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03653936
Acronym
KY
Enrollment
63
Registered
2018-08-31
Start date
2018-04-01
Completion date
2018-11-30
Last updated
2019-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wave Form Signals Coming From the Eye in a Healthy Cohort

Brief summary

Rebion (Rebiscan, Inc) has developed a noninvasive, handheld device that uses retinal birefringence scanning (RBS) to rapidly assess eye fixation and retinal integrity in adults and children. The proprietary technology uses a scanned annulus of polarized laser light to create a signature that confirms central fixation within seconds. The project described herein aims to provide accurate assessment of brain dysfunction in TBI (Traumatic Brain Injury) patients through the use of the developed device, which is called the Head and Intraocular Trauma Test (HITT) device.

Interventions

Rebion has developed a noninvasive, handheld device that uses retinal polarization scanning (RPS) to rapidly assess eye fixation and retinal integrity in adults and children. RPS can automatically detect the fixation of the human eye with proprietary technology that uses a scanned annulus of polarized laser light to create a signature that confirms central fixation within seconds. RPS requires no calibration or imaging, and eye movement recordings are not required. The HITT device is a repurposed Pediatric Vision Scanner (PVS), Rebion's first commercial product which has passed all applicable safety and performance standards.

Sponsors

BlueGrass Orthopaedics Surgery & Hand Care
CollaboratorUNKNOWN
Rebiscan, Inc.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
11 Years to 21 Years
Healthy volunteers
Yes

Inclusion criteria

* Student-athletes who present to schools affiliated with the Bluegrass Sports Clinica * Engaged in sports * Older or equal to 11 years of age, and less than 21 years of age. * Provide informed consent; youths must have their parents sign the informed consent document. Children will be presented with a written assent statement and that they will be asked to sign the assent document.

Exclusion criteria

* Catastrophic polytrauma that would interfere with follow-up and outcome assessment * Amblyopia/strabismus * Pregnancy in female subjects * Any injury to eye including, puncture, scratch, occlusion, fracture to orbital socket (or any fracture to face that would negatively impact eye movement/vision) that would interfere with ability to complete study-device assessment. * History of poor vision prior to injury (Visual acuity worse than 20/40 in either eye) * Intoxication or chemical impairment at time of examination (upon initial presentation)

Design outcomes

Primary

MeasureTime frameDescription
Capturing of wave forms from the eyeScreenings will be performed during a normally scheduled visit to the sports facility by the research group enrolling in the studyScreening device will provide a wave form calculation of light reflecting off patient's eye

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026