Tiny genetic clues may unlock eye disease mysteries
NCT ID NCT04658251
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at people with cone disorders, a type of inherited eye disease that affects color vision and sharp sight. Researchers analyzed genetic changes of unknown significance to see if they cause disease. The goal was to improve genetic diagnosis, not to test a treatment. Only 7 people took part before the study ended early.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CHU lille
Lille, 59037, France
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Other studies related to the condition(s) this trial covers.
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