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Developing Vision Tests for Adults With Inherited Retinal Disease and Low Vision

Develops and evaluates vision tests in adults with inherited retinal disease and low vision.

Plain-language title generated from the registry record
Registry title: Development and Evaluation of Functional Visual Field and Navigation Endpoints in Moderate to Profound Inherited Retinal Disease (DEFINE-IRD)

Key facts

Where
Irvine, United StatesSee the site

Where in United States

  • Vision Research and Assessment InstituteIrvine, United StatesTaking people

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Trial details

Who runs it
Ray Therapeutics, Inc.
Trial code
NCT07502664
Record updated
31 March 2026
Original description
The Vision Research and Assessment Institute (VRAI) was established with the purpose of serving as a testing facility for efficacy endpoints for patients with Low Vision.Read full original descriptionShow less

Development and Evaluation of Functional Visual Field and Navigation Endpoints in Moderate to Profound Inherited Retinal Disease (DEFINE-IRD)

The Vision Research and Assessment Institute (VRAI) was established with the purpose of serving as a testing facility for efficacy endpoints for patients with Low Vision.

The mission of the VRAI is to enable the highest quality, standardized efficacy testing of patients with visual impairment.

The VRAI facilitates the development and refinement of existing endpoints specifically for testing patients with Low Vision.

Inclusion: Diagnosis of bilateral retinitis pigmentosa (RP) or other retinal dystrophies impacting peripheral vision as confirmed from previous eye examination records; Best-corrected visual acuity between 20/200 to HM in at least one eye; Reasonably fluent in English or Spanish.

Exclusion: Cognitive impairment, memory loss or dementia sufficient in severity to preclude informed consent or in the opinion of the investigator would prevent satisfactory completion of some or all of the testing; Any circumstance that in the opinion of the investigator, would interfere with participation in, or compliance with the study protocol; Current pregnancy as reported by patient.

ClinicalTrials.gov NCT07502664