Cone dystrophy
MONDO:0000455An inherited ocular disorder characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision.
Also known as: cone dystrophy, progressive cone dystrophy, stationary cone dystrophy, retinal cone dystrophy
28 clinical trials for this condition and its sub-types, 4 tagged with Cone dystrophy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Cone dystrophy
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Cone dystrophy 3 0 trials
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Cone dystrophy 4 0 trials
1 sub-type
- Achromatopsia 5 0 trials
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Retinal cone dystrophy 4 0 trials
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Retinal cone dystrophy type 1 0 trials
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Could stem cells restore sight in damaged eyes?
Disease control Recruiting nowThis study tests whether injecting a person's own bone marrow stem cells into or near the eye can help treat various retinal and optic nerve diseases, including age-related macular degeneration, retinitis pigmentosa, and glaucoma. Participants receive stem cell injections via dif…
Sponsor: MD Stem Cells • Aim: Disease control
Last updated Jul 01, 2026 00:00 UTC
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Thousands join fight against blindness by sharing their stories
Knowledge-focused Recruiting nowThis registry collects information from people with inherited retinal diseases, like retinitis pigmentosa and Stargardt disease. Participants share their symptoms, family history, and genetic test results online. The goal is to help researchers understand these rare diseases and …
Sponsor: Foundation Fighting Blindness • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:36 UTC
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New eye scans could revolutionize how we see retinal disease
Knowledge-focused Recruiting nowThis study uses special cameras to take ultra-detailed pictures of the back of the eye in people with retinal diseases like macular degeneration and retinitis pigmentosa. Researchers aim to develop new ways to diagnose and track these conditions by measuring cell density and func…
Sponsor: Food and Drug Administration (FDA) • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:30 UTC