Clinical Trials on Brain Diseases, Metabolic, Inborn

Total 824 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
    • 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
    • NCT04675749
      Recruiting
      Conditions: X-linked Adrenoleukodystrophy
    • NCT03233841
      Completed
      Conditions: Farber Disease; Farber's Disease; Farber Lipogranulomatosis; Acid Ceramidase Deficiency; Ceramidase Deficiency; N-Laurylsphingosine Deacylase Deficiency; ASAH1 Mutation
    • NCT04602325
      Recruiting
      Conditions: Urea Cycle Disorder; Organic Acidemia; Maple Syrup Urine Disease; Glutaric Acidemia I; Fatty Acid Oxidation Disorder; Hypoxic-Ischemic Encephalopathy
    • NCT01341379
      Withdrawn
      Conditions: Urea Cycle Disorders, Inborn; Inborn Errors of Metabolism; Propionic Acidemia; Methylmalonic Acidemia; Carbamyl Phosphate Synthetase Deficiency
    • NCT04248062
      Completed
      Conditions: Inborn Errors of Metabolism; Urea Cycle Disorder; Maple Syrup Urine Disease; Phenylketonurias; Methylmalonicacidemia; OTC Deficiency; Aminoacidopathy; Patient Reported Outcome Measurements
    • NCT01780168
      Recruiting
      Conditions: Oxidative Phosphorylation Deficiencies; Electron Transport Chain Disorders, Mitochondrial; Mitochondrial Disorders; Leigh Disease
    • NCT00668564
      Terminated
      Conditions: Hurler's Syndrome; Maroteaux-Lamy Syndrome; Sly Syndrome; Alpha Mannosidosis; Fucosidosis; Aspartylglucosaminuria; Sphingolipidoses; Krabbe Disease; Wolman's Disease; Niemann-Pick Disease Type B; Niemann-Pick Disease, Type C
    • NCT00176904
      Completed
      Conditions: Adrenoleukodystrophy; Metachromatic Leukodystrophy; Globoid Cell Leukodystrophy; Gaucher's Disease; Fucosidosis; Wolman Disease; Niemann-Pick Disease; Batten Disease; GM1 Gangliosidosis; Tay Sachs Disease; Sandhoff Disease
    • NCT00007020
      Completed
      Conditions: Infantile Refsum's Disease; Zellweger Syndrome; Adrenoleukodystrophy; Peroxisomal Disorders; Cholestasis
    • NCT02297347
      Completed
      Conditions: Phenylketonuria
    • NCT00004307
      Unknown status
      Conditions: Amino Acid Metabolism, Inborn Errors
    • NCT01917344
      Completed
      Conditions: Phenylketonuria
    • NCT02410239
      Withdrawn
      Conditions: Cerebral Adrenoleukodystrophy
    • NCT03911089
      Active, not recruiting
      Conditions: Urea Cycle Disorder; Inborn Errors of Metabolism
    • NCT02948062
      Withdrawn
      Conditions: Adrenoleukodystrophy
    • NCT04204642
      Recruiting
      Conditions: Cerebral Amyloid Angiopathy
    • NCT00964236
      Completed
      Conditions: Phenylketonuria
    • NCT04528706
      Recruiting
      Conditions: Cerebral Adrenoleukodystrophy
    • NCT03168399
      Completed
      Conditions: Phenylketonuria; Inborn Errors of Metabolism
    • NCT03058848
      Completed
      Conditions: Phenylketonuria; Inborn Errors of Metabolism
    • NCT03852498
      Recruiting
      Conditions: Cerebral Adrenoleukodystrophy (CALD)
    • NCT02124330
      Completed
      Conditions: Urea Cycle Disorders, Inborn; Other Metabolic Diseases