Hospital Universitario de la Paz
Hospital Universitario de la Paz
Madrid, Madrid, Spain4 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| A Study of Migalastat in Pediatric Subjects (2 to <12 Yrs) With Fabry Disease and Amenable GLA Variants | Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Cerebral Small Vessel Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Fabry disease, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Nutritional and Metabolic Diseases, X-linked disease, brain disorder, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, hereditary disease, inborn errors of metabolism, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, nervous system disorder, sphingolipidosis, vascular disorder | Recruiting | Phase 3 | 2026-09-01 | NCT06904261 | |
| Anatomy-based Fitting in Cochear Implant Users | Cochlear Implant; Outcomes; Quality of Life | Recruiting | Not applicable | 2025-08-12 | NCT05360212 | |
| Analysis of Musical and Voice Skills in Children and Adult Cochlear Implant Users | Cochlear Implant; Music; Voice | Recruiting | Not stated | 2025-08-12 | NCT05319678 | |
| Abbott Vascular Medical Device Registry | Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, X-linked disease, acute myocardial infarction, brain disorder, cardiovascular disorder, central nervous system disorder, coronary artery disorder, coronary restenosis, coronary stenosis, heart disorder, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, myocardial ischemia, nervous system disorder, ornithine carbamoyltransferase deficiency, urea cycle disorder, vascular disorder | Recruiting | Not stated | 2025-07-03 | NCT04573660 |