Brittle bone disease registry opens to track 5,000 patients
NCT ID NCT04115774
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is a registry that gathers medical, genetic, and quality-of-life information from people with osteogenesis imperfecta (brittle bone disease). It aims to track how the disease progresses over time and how different genetic changes affect symptoms. No new treatments are being tested. The registry is currently only open to people living in Italy.
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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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Irccs Istituto Ortopedico Rizzoli
RECRUITINGBologna, Emilia-Romagna, 40136, Italy
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Other studies related to the condition(s) this trial covers.
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