IRCCS Istituto Ortopedico Rizzoli
IRCCS Istituto Ortopedico Rizzoli
Bologna, Emilia-Romagna, Italy8 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Efficacy of Robot-assisted Technique vs Conventional Technique in Preventing Early Micromobilisation After UKA | Pathologic Processes, Pathological Conditions, Signs and Symptoms, Postoperative Complications, Prosthesis Failure, Prosthesis Loosening | Active, not recruiting | Not applicable | 2026-01-23 | NCT05204797 | |
| Prospective Observational Cohort Study of Cardiac Structure and Function in Children and Adults With Osteogenesis Imperfecta | Bone 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 imperfecta | Recruiting | Not stated | 2025-12-17 | NCT07287241 | |
| Data Collection of Patients With Rare Bone Diseases | Congenital, 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 dysplasia | Recruiting | Not stated | 2025-11-20 | NCT05247645 | |
| Registry of Li Fraumeni and Li Fraumeni Like Syndromes | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA repair disease, Li-Fraumeni syndrome, Li-fraumeni-like syndrome, Nutritional and Metabolic Diseases, hereditary disease, hereditary neoplastic syndrome, metabolic disease, neoplasm | Recruiting | Not stated | 2025-11-20 | NCT04982744 | |
| Registry of Ollier Disease and Maffucci Syndrome | Bone Diseases, Developmental, Enchondromatosis, Maffucci syndrome, bone disorder, musculoskeletal system disorder, osteochondrodysplasia | Recruiting | Not stated | 2025-11-20 | NCT04134572 | |
| Registry of Multiple Osteochondromas | Bone 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, osteochondrodysplasia | Recruiting | Not stated | 2025-11-20 | NCT04133285 | |
| Registry of Ehlers-Danlos Syndrome | Collagen 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 disease | Recruiting | Not stated | 2025-11-20 | NCT04133272 | |
| Registry of Osteogenesis Imperfecta | Bone 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 imperfecta | Recruiting | Not stated | 2025-11-20 | NCT04115774 |