LCA5-related retinopathy
MONDO:0100445A retinopathy caused by biallelic variants in the LCA5 gene.
Also known as: LCA5 retinopathy, LCA5-related retinopathy, LCA5, LCA5 Leber congenital amaurosis, Leber congenital amaurosis 5, Leber congenital amaurosis caused by mutation in LCA5, Leber congenital amaurosis type 5, amaurosis congenita of Leber, type 5
27 clinical trials for this condition and its sub-types, 1 tagged with LCA5-related retinopathy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of LCA5-related retinopathy
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Leber congenital amaurosis 5 2 trials
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VR headsets tested as a possible treatment for blindness
Disease control Stopped earlyThis study tested whether using a virtual reality headset for one-hour sessions could help regenerate damaged optic nerves and improve vision in people with glaucoma or other retinal diseases. The idea came from promising results in rodents. However, the trial was terminated earl…
Sponsor: Stanford University • Aim: Disease control
Last updated Jun 27, 2026 08:03 UTC
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Scientists dig into DNA to unravel rare eye disorders
Knowledge-focused Stopped earlyThis study looked at over 100 people with inherited retinal dystrophies, a group of rare eye diseases that can cause vision loss. Researchers collected genetic and eye exam data to find links between specific gene mutations and symptoms. The goal was to better understand these di…
Sponsor: Fondation Ophtalmologique Adolphe de Rothschild • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:03 UTC