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Clinical Trials/NCT03653936
NCT03653936CompletedNot Applicable

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

Rebiscan, Inc.1 site in 1 country63 target enrollmentStarted: April 1, 2018Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
63
Locations
1
Primary Endpoint
Capturing of wave forms from the eye

Study Overview

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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
11 Years to 21 Years (Child, Adult)
Sex
All
Accepts 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)

Outcomes

Primary Outcomes

Capturing of wave forms from the eye

Time Frame: Screenings will be performed during a normally scheduled visit to the sports facility by the research group enrolling in the study

Screening device will provide a wave form calculation of light reflecting off patient's eye

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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