CHU Saint-Etienne
CHU Saint-Etienne
Saint-Priest-en-Jarez, France4 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Prospective, Longitudinal, Observational Registry of Adult Patients With Hypophosphatasia (REG-HYPO) | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Tendon Injuries, disease of the tendon, enthesopathy, hereditary disease, hypophosphatasia, inborn errors of metabolism, inborn metal metabolism disorder, injury, metabolic disease, muscle tissue disorder, musculoskeletal system disorder | Recruiting | Not stated | 2026-08-05 | NCT05596539 | |
| Justification of the Initial Diagnosis and Evaluation of the Overall Evolution of a Cohort of Recent Polymyalgia Rheumatica (JADORE) | Bacterial Infections and Mycoses, Infections, Skin and Connective Tissue Diseases, arthritic joint disease, arthropathy, bacterial infectious disease, connective tissue disorder, gram-positive bacterial infections, muscle tissue disorder, musculoskeletal system disorder, polymyalgia rheumatica, rheumatic disorder, rheumatic fever, streptococcal infection | Not yet recruiting | Not stated | 2026-06-08 | NCT07132164 | |
| Efficacy of Regorafenib Combined With Best Supportive Care as Maintenance Treatment in High Grade Bone Sarcomas Patients | Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Bone Tissue, Neoplasms, Connective and Soft Tissue, bone disorder, bone sarcoma, connective tissue neoplasm, musculoskeletal system disorder, neoplasm, osteosarcoma, sarcoma | Recruiting | Phase 2 | 2026-02-17 | NCT04698785 | |
| Safety of Trifluridine/Tipiracil in Patients With Dihydropyrimidine Dehydrogenase Deficiency Diagnosed With Metastatic Colorectal or Gastroesophageal Cancer | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Digestive System Neoplasms, Neoplasms by Site, Nutritional and Metabolic Diseases, colonic disorder, colorectal neoplasm, digestive system disorder, digestive system neoplasm, dihydropyrimidine dehydrogenase deficiency, hereditary disease, inborn disorder of purine or pyrimidine metabolism, inborn errors of metabolism, intestinal disorder, metabolic disease, neoplasm, rectal disorder | Recruiting | Phase 2 | 2025-12-10 | NCT06245356 |