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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Functional and Morphological Characterization of Multiple Osteochondromas DisorderBone Diseases, Developmental, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Exostoses, Neoplasms by Histologic Type, Neoplasms, Bone Tissue, Neoplasms, Connective and Soft Tissue, Ollier disease, Osteochondroma, bone disorder, connective tissue neoplasm, hereditary disease, hereditary multiple osteochondromas, hereditary neoplastic syndrome, hyperostosis, musculoskeletal system disorder, neoplasm, osteochondrodysplasiaRecruitingNot stated2026-03-24NCT06703736

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OrganizationsLinked trials
Istituto Ortopedico Rizzoli113

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Research sitesCityCountryLinked trials
IRCCS Istituto Ortopedico RizzoliBolognaItaly26