Scientists watch brittle bone disease in kids to unlock its secrets
NCT ID NCT03575221
First seen Nov 01, 2025 · Last updated May 20, 2026 · Updated 28 times
Summary
This study followed 46 children with osteogenesis imperfecta (OI), a condition that causes fragile bones and short stature, to understand how the disease progresses and how genes influence it. Participants had regular check-ups, scans, and tests over several years. No treatments were tested; the goal was simply to learn more about OI.
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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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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Genom att skicka in godkänner du våra Användarvillkor
Locations
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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
Conditions
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