Visual Function Tests in Age-related Macular Degeneration

ORA, Inc.200 enrolled

Overview

The goal of this study is to assess a battery of visual function tests in subjects with non-exudative age-related macular degeneration

Age-related macular degeneration (AMD) is one of the leading causes of visual impairment among elderly populations in developed countries. Majority of AMD patients (80%) suffer from the dry or non-exudative form of the disease. Currently there are no approved treatments for dry AMD. Clinical development of therapeutic agents for dry AMD is limited by slow progressing nature of the disease as well as the lack of sensitive endpoints to assess therapeutic efficacy. Visual acuity, the commonly used functional endpoint, remains minimally affected during early stages of dry AMD. Thus novel visual function endpoints, that can identify functional deficits during early stages of dry AMD prior to development of geographic atrophy, are needed. In the current study a battery of visual function tests will be evaluated in subjects with different stages of dry AMD and normal controls, to assess their sensitivity and feasibility as potential functional endpoints for dry AMD.

Study Type

OBSERVATIONAL

Enrollment

200

Conditions

Age Related Macular Degeneration

Interventions

Visual Function TestsOTHER

All subjects will undergo a battery of visual function tests

Eligibility

Sex: ALLMin age: 60 YearsMax age: 99 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * All Subjects Must: 1. Be 60 years of age or older; 2. Provide written informed consent; 3. Be willing and able to follow all instructions and attend the study visits; 4. Must be able to perform all study procedures; Normal Subjects: 5. Have BCVA of 20/25 or better in the study eye; 6. Have no history or clinical evidence of AMD, retinal diseases or any other ocular pathologies in either eye; AMD Subjects: 7. Have BCVA of 20/40 or better in the study eye; 8. Have a clinical diagnosis of non-exudative AMD in the study eye; Exclusion Criteria: All subjects must not have any of the below criteria  1. Have a diagnosis of wet AMD in the study eye; 2. Have any other hereditary or acquired retinal diseases in either eye ; 3. Have glaucoma or other optic nerve diseases in either eye; 4. Have corneal or other anterior segment diseases in either eye; 5. Have significant cataract in the study eye; 6. Have a history of ocular trauma or ocular surgery (other than cataract removal) in the study eye; 7. Have a history of uncontrolled systemic disease (e.g. poorly controlled hypertension or poorly controlled diabetes); 8. Have a history of seizures; 9. On psychotropic medications; 10. Any other symptoms or conditions that could, in the opinion of the investigator, interfere with study procedures.

Locations (1)

Andover Eye Associates

Andover, Massachusetts, United States

Outcomes

Primary Outcomes

Critical flicker fusion

Critical flicker fusion will be tested using a computer based test for different stimulus colors, white, red, green and blue. A wide range of luminance and contrast levels will be tested. The subject would be seated in front of the monitor. The non-study eye will be occluded. Subjects would be given adequate practice tests prior to performing the actual test. The stimulus will be presented on the monitor screen and the subject indicates perceiving the stimulus by pressing a test button.

Time frame: At study visit through study completion, an average of 2 years

Secondary Outcomes

Dark adaptation

Dark adaptation function will be assessed with dilated pupils using computer based stimuli following photo bleach. Subject will be seated in front of the test monitor with best correction in place for the study eye. The subject will be instructed to keep fixating on a red fixation cross in the center of the monitor and respond to perceiving the stimulus presented by pressing the response trigger button. All stimuli will be presented in random order for all intensities presented. The stimulus intensity is programmed to decrease in intensity with time. The test will be terminated after 20 minutes of recording. Dark adaptation curve will be generated and rod-cone recovery time (in minutes) will be derived from the curve.

Time frame: At study visit through study completion, an average of 2 years

Reading Tests

Reading tests will be performed using an electronic tablet device. The subject will be seated in a comfortable position with the non-tested eye occluded. The tablet will be set up in a table right in front of the subject at a viewing distance of 40cm. The subject will be given detailed instructions on the test procedures and outcomes. The goal of this test to assess reading speed of the study eye under a variety of conditions such as high contrast-high luminance, low contrast, low luminance, crowded letters, pepper words of different lengths and vanishing optotypes. Each challenge will be tested using a different passage of similar difficulty level. For each passage, reading speed will be estimated as the time taken to accurately read the entire passage and recorded in words per minute (WPM).

Data from ClinicalTrials.gov

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