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Achromatopsia 3

MONDO:0009875

Any achromatopsia in which the cause of the disease is a mutation in the CNGB3 gene.

Also known as: ACHM3, CNGB3 achromatopsia, achromatopsia 3, achromatopsia caused by mutation in CNGB3, achromatopsia type 3, ACHM1 (formerly), ACHM1, formerly, RMCH1 (formerly)

30 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neuromuscular disease (98) Eye disorder (97) Vision disorder (85) Retinal disorder (79) Perceptual disorders (21) Human disease (14) Hereditary neurological disease (5)

Trials to join now! 17 Not yet recruiting 3 Not yet finished but already full! 4 Completed 5 Terminated 1

VR headsets tested as a possible treatment for blindness

Disease control Terminated

This 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…

Phase: NA • Sponsor: Stanford University • Aim: Disease control

Last updated Jun 27, 2026 08:03 UTC

Achromatopsia 3

Broader categories

VR headsets tested as a possible treatment for blindness