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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Data Collection of Patients With Rare Bone DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, connective tissue disorder, cutaneous mucinosis, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, mucopolysaccharidosis type 4, skeletal dysplasiaRecruitingNot stated2025-11-20NCT05247645
Registry of Ollier Disease and Maffucci SyndromeBone Diseases, Developmental, Enchondromatosis, Maffucci syndrome, bone disorder, musculoskeletal system disorder, osteochondrodysplasiaRecruitingNot stated2025-11-20NCT04134572
Registry of Multiple OsteochondromasBone 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 stated2025-11-20NCT04133285
Registry of Ehlers-Danlos SyndromeCollagen Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Ehlers-Danlos syndrome, Hemic and Lymphatic Diseases, Skin Abnormalities, Skin and Connective Tissue Diseases, cardiovascular disorder, connective tissue disorder, hematologic disorder, hemorrhagic disease, hereditary disease, hereditary skin disorder, skin disorder, vascular disorder, vascular hemostatic diseaseRecruitingNot stated2025-11-20NCT04133272
Registry of Osteogenesis ImperfectaBone Diseases, Developmental, Collagen Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, bone disorder, connective tissue disorder, hereditary disease, musculoskeletal system disorder, osteochondrodysplasia, osteogenesis imperfectaRecruitingNot stated2025-11-20NCT04115774