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Osteogenesis imperfecta (OI) is a rare genetic disorder of increased bone fragility and low bone mass. It is conceivable that children and adolescents with OI are less active than healthy peers becaus...
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Lead Sponsor
Hospices Civils de Lyon
NCT07366086 · Osteogenesis Imperfecta
NCT07412782 · Osteogenesis Imperfecta, Osteoporosis, and more
NCT04152551 · Osteogenesis Imperfecta
NCT05317637 · Osteogenesis Imperfecta
NCT03706482 · Osteogenesis Imperfecta
Centre de Référence des Maladies Rénales Rares - Hospices Civils de Lyon - Service de Néphrologie et Rhumatologie Pédiatriques - Hôpital Femme Mère Enfant
Bron
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Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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