Vision Improvement for Patients With Age-Related Macular Degeneration

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50-100
SponsorVIS, Inc.

About this trial

This study is being conducted to assess the safety and efficacy of the VIS, LLC (VIS) Opti-K Low Vision Aid Device and treatment to provide vision improvement to patients with age-related macular degeneration.

Eligibility criteria

Qualifiers

Male or Female

Any race

Patient is at least 50 years old.

Patient has diagnosed end stage dry or wet age-related macular degeneration in one or both eyes, as verified by a complete ocular examination.

Disqualifiers

Corneal disease or corneal disorder in either eye.

Pathological retinal morphology in either eye that completely affects the entire 10° (3 mm diameter) of the retina centered on the foveola.

Gonzalez-Markowitz chart Potential Visual Acuity (PVA) in the eye to be treated that is not improved by at least four lines compared to CDVA;

Increased IOP (above 20 mm Hg), glaucoma or history of glaucoma;

Trial design

Treatments tested in this trial

  • Vision Improvement

Treatment groups

200 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators