Clin2
NCT06435000Possibly a fitRecruiting

A study tracking Stargardt disease progression

StargardtStargardt's DiseaseStargardt DiseaseSTGD1

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

This study follows people with Stargardt disease (a genetic eye condition that causes vision loss) over time. It aims to learn more about how the disease progresses and does not test any treatment.

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

Phase
N/A
Enrollment
75 people
Ages
12 years to 65 years
Study type
Observational

Who can take part

  • You are 12 to 65 years old.
  • You have Stargardt disease type 1 (STGD1) caused by changes in both copies of the ABCA4 gene.
  • Your vision has gotten worse in the last 2 years.
  • Your best corrected vision in the study eye is between 20/20 and 20/320.
  • You have not had certain eye surgeries or taken vitamin A supplements recently.

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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