Hôpital Femme Mère Enfant
Hôpital Femme Mère Enfant
Bron, France5 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Long Term Follow-up of the TREOCAPA Study (TREOCAPA-LT) | Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases and Pregnancy Complications, Obstetric Labor Complications, Obstetric Labor, Premature, Premature Birth, Urogenital Diseases, cardiovascular disorder, congenital heart disease, heart disorder, patent ductus arteriosus, pregnancy disorder | Recruiting | Not stated | 2026-04-16 | NCT06064825 | |
| Impact of First-trimester Preeclampsia Screening on Perinatal and Maternal Morbidity (RANSPRE) | Female Urogenital Diseases and Pregnancy Complications, Urogenital Diseases, hypertension, pregnancy-induced, preeclampsia, pregnancy disorder | Recruiting | Not applicable | 2026-03-27 | NCT05521776 | |
| Food-related Quality of Life in Patients With Cancer | Cancer of Gastrointestinal Tract, Digestive System Diseases, Digestive System Neoplasms, Head and Neck Neoplasms, Neoplasms by Site, Skin and Connective Tissue Diseases, Thoracic Neoplasms, breast cancer, breast disorder, breast neoplasm, digestive system disorder, digestive system neoplasm, female reproductive organ cancer, lung cancer, lung disorder, lung neoplasm, neoplasm, respiratory system disorder, respiratory tract neoplasm, skin disorder | Not yet recruiting | Not stated | 2026-02-27 | NCT07437326 | |
| An Extension Study of JR-141 to Evaluate the Long-term Safety and Efficacy in MPS II (Hunter Syndrome) Subjects | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, X-linked disease, connective tissue disorder, cutaneous mucinosis, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inherited neurodegenerative disorder, intellectual disability, lysosomal storage disease, metabolic disease, mucopolysaccharidosis, mucopolysaccharidosis type 2, nervous system disorder | Enrolling by invitation | Phase 3 | 2026-01-21 | NCT05594992 | |
| Is CYP24A1 Heterozygosity a Risk Factor for Nephrolithiasis? | Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Urogenital Diseases, calcinosis, calcium metabolic disease, kidney disorder, metabolic disease, nephrocalcinosis, nephrolithiasis, urinary system disorder, urolithiasis | Not yet recruiting | Not stated | 2025-12-02 | NCT07201701 |