Stargardt-like Macular Dystrophy (STDG3) Secondary to Mutations in ELOVL4

🩺 Protocol Summary

Background: STDG3 is an inherited eye disease. Currently there is no treatment for STDG3. Past studies of STDG3 have largely looked at members of large families at a single time point. Researchers want to learn more about the disease at an individual level. Objective: To understand the natural history of changes in the retina that occur in people with STDG3. Eligibility: People ages 10 and older with STDG3 due to a variant in the ELOVL4 gene. Design: Participants will have 6 visits. First they will have a screening visit, followed by a baseline visit. Then they will have a visit 6 months later. Then they will have a visit 1, 2, and 3 years after the first visit. Visits will last 4 to 8 hours. Visits will include the following: Medical history and physical exam. Complete eye exam. Participants' eye pressure and ability to see letters on a vision chart will be tested. Their pupils will be dilated with eye drops. Pictures will be taken of the retina and the inside of the eye. Questions about participants' family history, especially the presence of eye disease. Visual field test. Participants will be seated in front of a large dome and asked to press a button when they see a light within the dome. Electroretinogram. Participants will sit in the dark with their eyes patched for 30 minutes. Then they will wear special contact lenses and watch flashing lights. Optical coherence tomography. Cross-sectional pictures will be taken of participants' retinas. Fundus autofluorescence. Blue light will be shone into participants eyes to assess the health of the retina....

Primary Research Facility: National Institutes of Health Clinical Center (Bethesda, Maryland)

Review these 3 basic logistical and protocol criteria extracted from the public NIH record. (This is a preliminary logistical checklist, not an official clinical eligibility determination).

Diagnosed with, undergoing evaluation for, or seeking treatment related to Stargardt-Like Macular Dystrophy?

🔍 Study Population / Focus Area (Source: Protocol Primary Condition)

Aged between 10 Years and 100 Years?

🔍 Protocol Specified Age Range: 10 Years to 100 Years

Able to attend required clinic visits at National Institutes of Health Clinical Center (Bethesda, Maryland)?

🔍 Logistical Requirement: Site at National Institutes of Health Clinical Center

📍 Primary Site Map

Site: National Institutes of Health Clinical Center — Bethesda, Maryland

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