Stanmore

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Registry of Patients With Hypophosphatasia	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, hypophosphatasia, inborn errors of metabolism, inborn metal metabolism disorder, metabolic disease	Enrolling by invitation	Not stated	2026-09-04		NCT02306720
The Medacta International GMK Sphere Post-Marketing Surveillance Study	Necrosis, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Skin and Connective Tissue Diseases, arthritic joint disease, arthropathy, autoimmune disease, avascular necrosis, bone disorder, connective tissue disorder, immune system disorder, musculoskeletal system disorder, osteonecrosis, rheumatic disorder, rheumatoid arthritis	Active, not recruiting	Not applicable	2024-12-16		NCT02199600

Clinical trials