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An Early Prospective Study of the Traq™ Device for Characterization of Binocular Ocular Function in Normal Subjects and Subjects With Recent Traumatic Brain Injury

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

The early prospective study of Traq™ (an investigational binocular ophthalmic neurodiagnostic device) will measure binocular ocular functions (bilateral foveal fixation, foveal binocularity, and fovea-tracked saccadic latency) in normal subjects and those with history of mild-to moderate traumatic brain injury (mTBI).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 12
Healthy Volunteers: t
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• Age 12 years or older at the time of enrollment.

• Able to understand and sign an informed consent form (or with parent/guardian for subjects less than 18 years of age).

• Willing and able to complete all required study visits and test assessments.

• Subjects with no history of traumatic brain injury (normal arm).

• Subjects with a history of mild to moderate traumatic brain injury (mTBI) within the last six months, (post-TBI arm).

Locations
United States
Iowa
Elite Eye Care/Elite Vision Therapy
RECRUITING
Waukee
Contact Information
Primary
Justin Shaka
jgshaka@rebiscan.com
857-600-0982
Time Frame
Start Date: 2026-07-14
Estimated Completion Date: 2026-10
Participants
Target number of participants: 10
Treatments
Head trauma group
Subjects with history of head trauma within the prior 6 months
Controls
Subjects with no history of head trauma
Related Therapeutic Areas
Sponsors
Leads: Rebiscan, Inc.

This content was sourced from clinicaltrials.gov