Clin2
NCT07265895Possibly a fitNot yet recruiting

Inherited retinal disease study

Retinal DegenerationsRetinitis Pigmentosa (RP)Stargardt Disease

Part of Eyes & vision, Genetic & congenital clinical trials.

This study follows people with inherited retinal diseases to learn how these conditions progress and how genetic changes relate to symptoms. It may help improve future care and treatments.

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 have had at least one eye exam and retinal imaging at our center.
  • You have been diagnosed with an inherited retinal disease based on your family history, symptoms, or imaging.
  • You have a confirmed genetic diagnosis from a reliable genetic test.
  • You do not have other eye conditions like diabetic retinopathy or glaucoma.
  • You have not taken certain medications that can harm the retina, such as hydroxychloroquine or tamoxifen.

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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