Massive 5,000-Person study maps the journey of brittle bone disease
NCT ID NCT04115774
Summary
This study is creating a detailed health registry for people with Osteogenesis Imperfecta (brittle bone disease). It aims to collect and link information from up to 5,000 patients in Italy about their symptoms, treatments, genetics, and quality of life over time. The goal is to better understand how the disease progresses and how a person's genes relate to their symptoms, which could help guide future care and research.
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 Istituto Ortopedico Rizzoli
RECRUITINGBologna, Emilia-Romagna, 40136, Italy
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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