Vision Improvement for Legally Blind Dry AMD Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age50-100
SponsorOptimal Acuity Corporation

About this trial

This retrospective observational study is intended to assess the feasibility of using a nonsignificant risk device for vision improvement for legally blind dry AMD patients.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Male or Female

Any race

Patient is at least 50 years old.

Patient must have dry AMD in the study eye.

Disqualifiers

Visually significant cataract in the study eye

Presence of a visually significant posterior capsule opacity if prior cataract surgery has been performed in the study eye

Any visually significant disease process in any ocular structure other than AMD that would affect vision in the study eye

Previous corneal surgery in the study eye

Trial population

Patients with dry age-related macular degeneration an legal blindness in one or both eyes

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • Clear-K Low Vision Aid Treatment

    Device

    A Clear-K Low Vision Aid Device is used to produce small corneal shape and refraction changes in order to redirect light onto functional areas of the retina.

Treatment groups

40 Participants
are divided into 1 treatment group
Group A: Legally Blind Dry AMD Patients1 intervention

Trial outcomes

Primary outcomes

1

Best spectacle-corrected distance visual acuity (BCDVA)

BCDVA measured using ETDRS eye charts

Time frame
12 months post-treatment

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: