iron poisoning
iron poisoning
Explore linked clinical trials. Standard reference: MONDO:080038515 results · Page 1 of 1
Clinical trials
Swipe the table sideways for more columns.
| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Efficacy and Safety of Vamifeport in Adult Participants With Homeostatic Iron Regulator Gene (HFE)-Related Hereditary Hemochromatosis | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, iron metabolism disease, iron poisoning, metabolic disease | Recruiting | Phase 2 | 2026-09-16 | NCT07332091 | |
| Fully Automated High-Throughput Quantitative MRI of the Liver | Digestive System Diseases, Nutritional and Metabolic Diseases, fatty liver disease, iron metabolism disease, iron poisoning, liver disorder, metabolic disease | Recruiting | Not stated | 2026-09-16 | NCT05294471 | |
| Apotransferrin in Atransferrinemia | Hemic and Lymphatic Diseases, Nutritional and Metabolic Diseases, anemia, atransferrinemia, hematologic disorder, iron metabolism disease, iron poisoning, metabolic disease | Active, not recruiting | Phase 2 | 2026-09-16 | NCT01797055 | |
| Treatment of Hemochromatosis | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, iron metabolism disease, iron poisoning, metabolic disease | Active, not recruiting | Phase 2 | 2026-09-16 | NCT00007150 | |
| Early Screening and Treatment of Heart Complication in Sickle Cell Disease | Arrhythmias, Cardiac, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, anemia, cardiomyopathy, cardiovascular disorder, familial hemolytic anemia, heart disorder, hematologic disorder, hemolytic anemia, hereditary disease, inherited hemoglobinopathy, iron metabolism disease, iron poisoning, metabolic disease, sickle cell disease | Recruiting | Phase 2 | 2026-09-09 | NCT07023666 | |
| Neurodegenerative Diseases Progression Markers (MARKERS-NDD) | Alzheimer disease, Cognition Disorders, Cognitive Dysfunction, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Frontotemporal Lobar Degeneration, Lewy body dementia, Neurologic Manifestations, Nutritional and Metabolic Diseases, Ocular Motility Disorders, Parkinson disease, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, TDP-43 proteinopathy, amyotrophic lateral sclerosis, autonomic nervous system disorder, basal ganglia disorder, brain disorder, central nervous system disorder, cognitive disorder, corticobasal degeneration disorder, cranial nerve neuropathy, dementia, eye disorder, hereditary disease, inherited neurodegenerative disorder, iron metabolism disease, iron poisoning, metabolic disease, motor neuron disorder, movement disorder, multiple system atrophy, nervous system disorder, neuroaxonal dystrophy, neurodegeneration with brain iron accumulation, neurodegenerative disease, neuromuscular disease, ophthalmoplegia, palsy, pantothenate kinase-associated neurodegeneration, parkinsonian disorder, primary dysautonomia, proteostasis deficiencies, psychiatric disorder, spinal cord disorder, synucleinopathy, tauopathy | Recruiting | Not stated | 2026-09-02 | NCT06596746 | |
| Impact of Transferrin Saturation Guided Maintenance Treatment on Quality of Life in HFE Haemochromatosis | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, hereditary hemochromatosis, inborn errors of metabolism, inborn metal metabolism disorder, iron metabolism disease, iron poisoning, metabolic disease | Active, not recruiting | Not applicable | 2026-06-12 | NCT04779593 | |
| A Study to Evaluate BBI-001 in Healthy Volunteers and in Patients With Hereditary Hemochromatosis | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, hereditary hemochromatosis, inborn errors of metabolism, inborn metal metabolism disorder, iron metabolism disease, iron poisoning, metabolic disease | Recruiting | Phase 1 / Phase 2 | 2026-05-13 | NCT07371793 | |
| Impact of Iron Overload on the Incidence of Liver Complications in Long-Term Survivors (≥10 Years) of Allogeneic Hematopoietic Stem-Cell Transplantation. | Digestive System Diseases, Fibrosis, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, cirrhosis of liver, graft versus host disease, hemosiderosis, immune system disorder, iron metabolism disease, iron poisoning, liver disorder, metabolic disease | Recruiting | Not stated | 2026-04-27 | NCT07028112 | |
| Evaluation of the Quality of Life in Patients With Chronic Iron Overload Due to Hemoglobinopathies in Greece. | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, Nutritional and Metabolic Diseases, anemia, familial hemolytic anemia, hematologic disorder, hemolytic anemia, hereditary disease, inherited hemoglobinopathy, iron metabolism disease, iron poisoning, metabolic disease, thalassemia | Not yet recruiting | Not stated | 2026-01-20 | NCT07352878 | |
| Ethnic Differences in Iron Absorption (FeGenes) | Anemia, Hypochromic, Hemic and Lymphatic Diseases, Iron Deficiencies, Nutritional and Metabolic Diseases, anemia, hematologic disorder, iron deficiency anemia, iron metabolism disease, iron poisoning, metabolic disease | Active, not recruiting | Not stated | 2025-08-06 | NCT04198545 | |
| Heme and Non-heme Iron Intakes, Gut Microbiota, and Influence on Host Iron Absorption | Anemia, Hypochromic, Hemic and Lymphatic Diseases, Iron Deficiencies, Nutritional and Metabolic Diseases, anemia, hematologic disorder, iron deficiency anemia, iron metabolism disease, iron poisoning, metabolic disease | Recruiting | Not stated | 2025-02-24 | NCT06146608 | |
| Leflunomide for Idiopathic Pulmonary Hemosiderosis in Children | Hemosiderosis, Pulmonary, Nutritional and Metabolic Diseases, hemosiderosis, iron metabolism disease, iron poisoning, lung disorder, metabolic disease, respiratory system disorder | Recruiting | Phase 1 / Phase 2 | 2023-07-10 | NCT05937191 | |
| An Observational Study Evaluating Patients With Chronic Liver Diseases Associated With Hepatic Steatosis | Cholangitis, Sclerosing, Chronic Disease, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Disease Attributes, Fibrosis, Hepatitis, Chronic, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, autoimmune disease, autoimmune hepatitis, bile duct disorder, biliary tract disorder, cholangitis, cholestasis, chronic pancreatitis, cirrhosis of liver, digestive system disorder, fatty liver disease, gastroenteritis, hepatitis, hereditary disease, immune system disorder, inborn errors of metabolism, inborn metal metabolism disorder, inflammatory bowel disease, intestinal disorder, intrahepatic cholestasis, iron metabolism disease, iron poisoning, liver disorder, metabolic disease, metabolic dysfunction-associated steatotic liver disease, pancreas disorder, pancreatitis, primary biliary cholangitis | Recruiting | Not stated | 2022-04-19 | NCT05335603 | |
| China Registry for Genetic / Metabolic Liver Diseases | Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Nutritional and Metabolic Diseases, Wilson disease, basal ganglia disorder, brain disorder, central nervous system disorder, hereditary disease, hereditary hyperbilirubinemia, inborn errors of metabolism, inborn metal metabolism disorder, inherited neurodegenerative disorder, iron metabolism disease, iron poisoning, liver disorder, metabolic disease, movement disorder, nervous system disorder, neurodegenerative disease | Recruiting | Not stated | 2017-04-27 | NCT03131427 |