Clinical Trials on Brain Diseases, Metabolic

Total 1169 results

    • NCT00472732
      Completed
      Conditions: Brain Diseases, Metabolic, Inborn; Urea Cycle Disorder; Ornithine Transcarbamylase Deficiency
    • NCT00237315
      Recruiting
      Conditions: Brain Diseases, Metabolic, Inborn; Amino Acid Metabolism, Inborn Errors; Urea Cycle Disorders
    • NCT03360656
      Recruiting
      Conditions: Stroke, Ischemic; Stroke Hemorrhagic; Fever; Seizures; Metabolic Encephalopathy
    • NCT03535142
      Recruiting
      Conditions: Non-Alcoholic Fatty Liver Disease; Metabolic Encephalopathy; Obesity, Morbid; Non-alcoholic Steatohepatitis
    • NCT02254863
      Recruiting
      Conditions: Adrenoleukodystrophy; Batten Disease; Mucopolysaccharidosis II; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Neimann Pick Disease; Pelizaeus-Merzbacher Disease; Sandhoff Disease; Tay-Sachs Disease; Brain Diseases, Metabolic, Inborn; Alpha-Mannosidosis; Sanfilippo Mucopolysaccharidoses
    • NCT03233841
      Completed
      Conditions: Farber Disease; Farber's Disease; Farber Lipogranulomatosis; Acid Ceramidase Deficiency; Ceramidase Deficiency; N-Laurylsphingosine Deacylase Deficiency; ASAH1 Mutation
    • NCT04675749
      Recruiting
      Conditions: X-linked Adrenoleukodystrophy
    • NCT02525887
      Terminated
      Conditions: Chronic Disease; Endocrine System Disease; Cardiovascular Disease; Respiratory Tract Disease; CNS Metabolic Disorders
    • NCT04519749
      Recruiting
      Conditions: Fabry Disease
    • NCT01923376
      Withdrawn
      Conditions: Hepatic Encephalopathy; HE; Cirrhosis; Altered Mental Status; AMS
    • NCT02171104
      Recruiting
      Conditions: Mucopolysaccharidosis Disorders; Hurler Syndrome; Hunter Syndrome; Maroteaux Lamy Syndrome; Sly Syndrome; Alpha-Mannosidosis; Fucosidosis; Aspartylglucosaminuria; Glycoprotein Metabolic Disorders; Sphingolipidoses; Recessive Leukodystrophies; Globoid Cell Leukodystrophy; Metachromatic Leukodystrophy; Niemann-Pick B; Niemann-Pick C Subtype 2; Sphingomyelin Deficiency; Peroxisomal Disorders; Adrenoleukodystrophy With Cerebral Involvement; Zellweger Syndrome; Neonatal Adrenoleukodystrophy; Infantile Refsum Disease; Acyl-CoA Oxidase Deficiency; D-Bifunctional Enzyme Deficiency; Multifunctional Enzyme Deficiency; Alpha-methylacyl-CoA Racmase Deficiency; Mitochondrial Neurogastrointestingal Encephalopathy; Severe Osteopetrosis; Hereditary Leukoencephalopathy With Axonal Spheroids (HDLS; CSF1R Mutation); Inherited Metabolic Disorders
    • NCT00931060
      Completed
      Conditions: Liver Diseases; Hepatic Encephalopathy; Hepatic Insufficiency
    • NCT01963650
      Terminated
      Conditions: Lipid Metabolism Disorders; Metachromatic Leukodystrophy (MLD); Nervous System Diseases; Brain Diseases; Central Nervous System Diseases; Demyelinating Diseases; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Sphingolipidoses; Hereditary Central Nervous System Demyelinating Diseases; Metabolic Inborn Brain Diseases; Lysosomal Storage Diseases; Metabolic Diseases; Sulfatidosis
    • NCT01372228
      Active, not recruiting
      Conditions: Hurler Syndrome (MPS I); Hurler-Scheie Syndrome; Hunter Syndrome (MPS II); Sanfilippo Syndrome (MPS III); Krabbe Disease (Globoid Leukodystrophy); Metachromatic Leukodystrophy (MLD); Adrenoleukodystrophy (ALD and AMN); Sandhoff Disease; Tay Sachs Disease; Pelizaeus Merzbacher (PMD); Niemann-Pick Disease; Alpha-mannosidosis
    • NCT02124330
      Completed
      Conditions: Urea Cycle Disorders, Inborn; Other Metabolic Diseases
    • NCT00309400
      Completed
      Conditions: Phenylketonuria; Galactosemia; Inborn Errors of Metabolism
    • NCT04318509
      Completed
      Conditions: PKU; Phenylketonurias; Inborn Errors of Metabolism; Metabolic Disease
    • NCT04309331
      Completed
      Conditions: PKU; Phenylketonurias; Inborn Errors of Metabolism; Metabolic Disease
    • NCT00001972
      Completed
      Conditions: Alzheimer's Disease; Brain Neoplasm; Niemann Pick Disease
    • NCT03284658
      Active, not recruiting
      Conditions: Tyrosinosis; Hepatorenal Tyrosinemia; Fumarylacetoacetase Deficiency; Fah Deficiency; Metabolic Disorders
    • NCT01043640
      Completed
      Conditions: Mucopolysaccharidosis; Hurler Syndrome; Hunter Syndrome; Maroteaux-Lamy Syndrome; Sly Syndrome; Alpha Mannosidosis; Fucosidosis; Aspartylglucosaminuria; Adrenoleukodystrophy (ALD); Krabbe Disease; Metachromatic Leukodystrophy (MLD); Sphingolipidoses; Peroxisomal Disorders
    • NCT03367546
      Recruiting
      Conditions: Sickle Cell Disease; Thalassemia; High Risk Hematologic Disorders; Cerebral Adrenoleukodystrophy; Inherited Metabolic Disorders
    • NCT02021266
      No longer available
      Conditions: Metachromatic Leukodystrophy
    • NCT03852498
      Recruiting
      Conditions: Cerebral Adrenoleukodystrophy (CALD)
    • NCT04248062
      Completed
      Conditions: Inborn Errors of Metabolism; Urea Cycle Disorder; Maple Syrup Urine Disease; Phenylketonurias; Methylmalonicacidemia; OTC Deficiency; Aminoacidopathy; Patient Reported Outcome Measurements