500 patients join quest to decode Fuchs' eye disease
NCT ID NCT05742321
First seen May 17, 2026 · Last updated Jun 17, 2026 · Updated 7 times
Summary
This study looks at how genes and symptoms are linked in Fuchs' corneal endothelial dystrophy, a common eye disease that affects the cornea. Researchers will analyze DNA from 500 people who need cornea surgery to find patterns that may explain why the disease looks different in different people. The goal is to better understand the disease, not to test a new treatment.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Study contacts
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Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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CHU Saint-Etienne
RECRUITINGSaint-Etienne, 42055, France
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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.