Massive data hunt launched to unlock secrets of rare bone disorders
NCT ID NCT05247645
Summary
This study aims to create a detailed registry of information from people with rare bone diseases, known as skeletal dysplasias. It will collect past and ongoing health data, including medical history, genetic information, and treatment details, from up to 1000 participants in Italy. The goal is to better understand how these diseases progress and how symptoms relate to a person's genetics, which could help improve future diagnosis and care.
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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
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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