Eye disease study aims to map vision loss to help future treatments
NCT ID NCT07265895
First seen Jan 07, 2026 · Last updated May 16, 2026 · Updated 21 times
Summary
This study looks at 200 people with inherited retinal diseases like retinitis pigmentosa and Stargardt disease. Researchers will review past eye exams and genetic tests to see how vision changes over time and how different genes affect the disease. The goal is to better understand these conditions so future clinical trials can be designed more effectively.
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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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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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IRCCS Ospedale San Raffaele
Milan, Italy, 20132, Italy
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.