Clin2
NCT05589714Possibly a fitRecruiting

Study your rare eye gene and track retinal disease over time

Inherited Retinal DegenerationRetinitis Pigmentosa

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

This study builds a registry and tracks the natural history of rare retinal dystrophies while also testing people for disease-causing gene variants. It may help researchers better understand what causes retinal degeneration and how it progresses.

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

Phase
N/A
Enrollment
1,500 people
Ages
4 years and older
Study type
Observational

Who can take part

  • You (or your child) are willing and able to consent and communicate during the study
  • You can complete the study’s check-in visits, questionnaires, and other screening tests
  • You must be age 4 or older
  • Genetic testing must show a rare disease-causing variant in a listed retinal dystrophy gene (from an approved lab)
  • Both eyes must have a retinal dystrophy diagnosis and allow clear eye photos for imaging
  • Your past eye health and treatments must not interfere with imaging or study measurements

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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