Clin2
NCT07085533Possibly a fitRecruiting

A Study of Inherited Retinal Diseases

Retinal DystrophiesColor Vision DefectsVision DisordersMacular DegenerationAchromatopsiaOptical Coherence Tomography (OCT)Visual AcuityGenotype

Part of Brain & nervous system, Eyes & vision clinical trials.

This study is looking at how inherited retinal diseases affect color vision over time. It may help researchers understand these conditions better and is a good fit for people with a known diagnosis who can describe what they see.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
200 people
Ages
Any age
Study type
Observational

Who can take part

  • You must be able to describe colors or see color test stimuli when asked.
  • You need a confirmed diagnosis of an inherited retinal disease (like retinitis pigmentosa).
  • You cannot have vision loss from other causes, such as optic nerve damage or brain problems.
  • You cannot have a condition that makes it hard to follow instructions or communicate clearly.
  • You cannot have had recent retinal surgery or treatments that could temporarily affect your retina.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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