A Performance Study Comparing the EyeMirage (Test Device) to Standard of Care (Reference Device) in Patients 18 to 65 Years of Age Undergoing Standard Eye Examinations Such as Visual Acuity, Visual Field, Color Vision, and Self-Paced Saccade for Various Conditions

This study will assess the effectiveness and accuracy of results of a new device for eye function testing. This will be done by comparing results of four eye tests that are done through the current standard used in eye clinics and that of this new device. Participants of this study will undergo the four eye tests using both the new device and the standard of care devices. The study will be done in one visit to the eye clinic. Thirty days after the eye tests were done, participants will be called by the clinic for a general follow-up and to discuss any problems, if needed.

NCT Number	NCT06908967
Lead Sponsor	Neuroptek Corporation Inc. Collaborators: St. Boniface Hospital, St. Boniface Hospital Asper Clinical Research Institute
Conditions	Visual Function
Enrollment	160 participants
Start Date	2025-06-13
Primary Completion	2026-02-24 (estimated)
Study Completion	2026-02-24 (estimated)
Updated on ClinicalTrials.gov	2026-03-12