RecruitingNCT07502664
Development and Evaluation of Functional Visual Field and Navigation Endpoints in Moderate to Profound Inherited Retinal Disease (DEFINE-IRD)
Sponsor
Ray Therapeutics, Inc.
Enrollment
25 participants
Start Date
Feb 19, 2026
Study Type
OBSERVATIONAL
Conditions
Summary
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.
Eligibility
Min Age: 18 Years
Inclusion Criteria3
- 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 Criteria3
- 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
Interested in this trial?
Get notified about updates and connect with the research team.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07502664
Related Trials
A Study to Learn How Stargardt-type Eye Conditions Progress in Children and Adults
NCT0742557412 locations
Rod and Cone Mediated Function in Retinal Disease
NCT026179661 location
Study of ALK-001 on the Progression of Stargardt Disease
NCT074193345 locations
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants
NCT0558971436 locations
Stem Cell Ophthalmology Treatment Study II
NCT030115414 locations