800 kids with rare eye defects tracked for 10 years – no treatment, just answers
NCT ID NCT05954403
First seen Feb 13, 2026 · Last updated May 15, 2026 · Updated 16 times
Summary
This study follows 800 children from birth to age 10 who have rare eye problems like missing eyes (anophthalmia), small eyes (microphthalmia), or other eye structure issues. Researchers will track vision, brain development, and overall health over time to better predict outcomes. No new treatments are being tested; the goal is to learn more about these conditions.
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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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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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RaDiCo-ACOEIL
RECRUITINGParis, Île-de-France Region, 75012, France
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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