Clinical Trials on Metabolism, Inborn Errors

Total 2237 results

    • NCT04098198
      Recruiting
      Conditions: Inborn Errors of Metabolism; Biomarker
    • NCT02322177
      Completed
      Conditions: Inborn Errors of Metabolism; Pregnancy; Acidemias
    • NCT04097275
      Recruiting
      Conditions: Inborn Errors of Metabolism
    • NCT03534752
      Completed
      Conditions: Inborn Errors of Metabolism
    • NCT01341379
      Withdrawn
      Conditions: Urea Cycle Disorders, Inborn; Inborn Errors of Metabolism; Propionic Acidemia; Methylmalonic Acidemia; Carbamyl Phosphate Synthetase Deficiency
    • NCT04201067
      Active, not recruiting
      Conditions: Congenital Disorders of Glycosylation
    • NCT00369421
      Recruiting
      Conditions: Arterial Calcification Due to CD73-Deficiency (ACDC)
    • 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
    • NCT04248062
      Completed
      Conditions: Inborn Errors of Metabolism; Urea Cycle Disorder; Maple Syrup Urine Disease; Phenylketonurias; Methylmalonicacidemia; OTC Deficiency; Aminoacidopathy; Patient Reported Outcome Measurements
    • NCT04645498
      Not yet recruiting
      Conditions: Covid19; Metabolism, Inborn Errors
    • NCT04308603
      Not yet recruiting
      Conditions: Non-Immune Hydrops Fetalis
    • NCT00004767
      Completed
      Conditions: Amino Acid Metabolism, Inborn Errors
    • NCT01780168
      Recruiting
      Conditions: Oxidative Phosphorylation Deficiencies; Electron Transport Chain Disorders, Mitochondrial; Mitochondrial Disorders; Leigh Disease
    • NCT00004307
      Unknown status
      Conditions: Amino Acid Metabolism, Inborn Errors
    • 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
    • NCT02707211
      Unknown status
      Conditions: Lipid Metabolism, Inborn Errors
    • NCT01141075
      Terminated
      Conditions: Amino Acid Metabolism, Inborn Errors
    • NCT00006061
      Completed
      Conditions: Methionine Adenosyltransferase Deficiency; Metabolism, Inborn Errors
    • NCT00654433
      Terminated
      Conditions: Inherited Metabolic Diseases; Lysosomal Storage Disorders; Peroxisomal Storage Diseases; Inborn Errors of Metabolism; Mucopolysaccharidosis
    • NCT00328159
      Completed
      Conditions: Inborn Errors of Metabolism
    • NCT03810690
      Withdrawn
      Conditions: Methylmalonic Acidemia (MMA); Metabolism, Inborn Errors
    • NCT00004481
      Completed
      Conditions: Lipid Metabolism, Inborn Errors; Sitosterolemia
    • NCT00099996
      Completed
      Conditions: Heart Diseases; Metabolism, Inborn Errors
    • NCT00010361
      Completed
      Conditions: Metabolism, Inborn Errors; Granulomatous Disease, Chronic
    • NCT00843921
      Active, not recruiting
      Conditions: Inborn Errors of Metabolism