200-Patient study aims to unlock secrets of rare bone disease
NCT ID NCT07569731
First seen May 21, 2026 · Last updated May 21, 2026
Summary
This study collects information from over 200 people with fibrous dysplasia, a rare bone condition that causes abnormal growths. Researchers will look at medical records, surgeries, and genetic data to better understand the disease and how it affects patients. No new treatments are being tested; the goal is simply to learn more about the condition.
Disclaimer
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This is a summary of
the original study
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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: •••••@•••••
Locations
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IRCCS Istituto Ortopedico Rizzoli
RECRUITINGBologna, BO, 40136, Italy
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.