Osteolysis, Essential
Osteolysis, Essential
Explore linked clinical trials. Standard reference: MESH:M00155374 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| A Prospective Natural History Study of Lymphatic Anomalies | Bone Diseases, Developmental, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Hemic and Lymphatic Diseases, Lymphatic Abnormalities, Osteolysis, Essential, Peritoneal Diseases, bone disorder, bone resorption disease, chylous ascites, digestive system disorder, intestinal disorder, lymphangiectasis, lymphatic system disorder, lymphedema, lytic metastatic bone lesion, musculoskeletal system disorder, protein-losing enteropathy | Recruiting | Not stated | 2026-09-28 | NCT05731141 | |
| Lymphatic Anomalies Registry for the Assessment of Outcome Data | Bone Diseases, Developmental, CLOVES syndrome, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Lymphatic Abnormalities, Osteolysis, Essential, angiomatosis, angioosteohypertrophic syndrome, blue rubber bleb nevus, bone disorder, bone resorption disease, cardiovascular disorder, kaposiform hemangioendothelioma, kaposiform lymphangiomatosis, lymphatic malformation, lymphatic malformation 12, lymphatic system disorder, lytic metastatic bone lesion, musculoskeletal system disorder, tufted angioma, vascular disorder, vascular malformation | Recruiting | Not stated | 2026-09-10 | NCT02399527 | |
| Pediatric Arthropathy Beyond Inflammation: Clinical Spectrum and Diagnostic Approach at Assiut University Children Hospital | Bone Diseases, Developmental, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Collagen Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Farber lipogranulomatosis, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Nutritional and Metabolic Diseases, Osteolysis, Essential, Osteolysis, Idiopathic Multicentric, Skin and Connective Tissue Diseases, bone disorder, bone resorption disease, brain disorder, central nervous system disorder, connective tissue disorder, cutaneous mucinosis, hereditary disease, hereditary skin disorder, hyaline fibromatosis syndrome, inborn carbohydrate metabolic disorder, inborn errors of metabolism, infantile systemic hyalinosis, lysosomal lipid storage disorder, lysosomal storage disease, lytic metastatic bone lesion, metabolic disease, mucopolysaccharidosis, musculoskeletal system disorder, nervous system disorder, osteochondrodysplasia, osteogenesis imperfecta, progressive pseudorheumatoid arthropathy of childhood, skin disorder, sphingolipidosis | Not yet recruiting | Not stated | 2025-09-15 | NCT07173010 | |
| Identification of Biomarkers for Patients with Vascular Anomalies | Bone Diseases, Developmental, CLOVES syndrome, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Osteolysis, Essential, angiomatosis, angioosteohypertrophic syndrome, bone disorder, bone resorption disease, cardiovascular disorder, diffuse lymphatic malformation, kaposiform hemangioendothelioma, kaposiform lymphangiomatosis, lytic metastatic bone lesion, musculoskeletal system disorder, vascular disorder, vascular malformation | Recruiting | Not stated | 2024-11-06 | NCT03001180 |