Clinical Trials on Lipid Metabolism, Inborn Errors

Total 709 results





    • NCT02707211
      Unknown status
      Conditions: Lipid Metabolism, Inborn Errors
    • NCT00092898
      Completed
      Conditions: Lipid Metabolism, Inborn Errors; Heart Disease
    • NCT00092820
      Completed
      Conditions: Lipid Metabolism, Inborn Errors; Heart Disease
    • NCT00092807
      Completed
      Conditions: Lipid Metabolism, Inborn Errors; Heart Disease
    • NCT00004481
      Completed
      Conditions: Lipid Metabolism, Inborn Errors; Sitosterolemia
    • NCT00092833
      Terminated
      Conditions: Hypercholesterolemia, Familial; Lipid Metabolism, Inborn Errors
    • NCT03198897
      Active, not recruiting
      Conditions: Lipoprotein Lipase Deficiency; Inborn Error of Lipid Metabolism; Corneal Arcus
    • NCT01782027
      Suspended
      Conditions: Cholesterol, HDL; Lipid Metabolism, Inborn Errors; Tangier Disease; LCAT Deficiency; Cholesteryl Ester Transfer Protein (CETP) Deficiency
    • NCT00260299
      Terminated
      Conditions: Mevalonic Aciduria; Mevalonate Kinase Deficiency; Immune System Diseases; Periodic Fever Syndromes, Hereditary; Lipid Metabolism, Inborn Errors
    • NCT01916512
      Unknown status
      Conditions: Low CETP Activity; CETP Deficiency; Hyperalphalipoproteinemia; Hyper-LDL-cholesterolemia; High Level of Remnant Cholesterol
    • NCT03393130
      Unknown status
      Conditions: Cognitive Impairment; Apolipoprotein E, Deficiency or Defect of; Critical Illness; Burns; Young Adult
    • NCT03531554
      Completed
      Conditions: VLCAD Deficiency; Fatty Acid Oxidation Defects
    • NCT01584206
      Completed
      Conditions: Sitosterolemia
    • NCT02635269
      Active, not recruiting
      Conditions: Metabolism, Inborn Errors; Lipid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency; Glycogenin-1 Deficiency (Glycogen Storage Disease Type XV); Carnitine Palmitoyl Transferase 2 Deficiency; VLCAD Deficiency; Medium-chain Acyl-CoA Dehydrogenase Deficiency; Multiple Acyl-CoA Dehydrogenase Deficiency; Carnitine Transporter Deficiency; Neutral Lipid Storage Disease; Glycogen Storage Disease Type II; Glycogen Storage Disease Type III; Glycogen Storage Disease Type IV; Glycogen Storage Disease Type V; Muscle Phosphofructokinase Deficiency; Phosphoglucomutase 1 Deficiency; Phosphoglycerate Mutase Deficiency; Phosphoglycerate Kinase Deficiency; Phosphorylase Kinase Deficiency; Beta Enolase Deficiency; Lactate Dehydrogenase Deficiency; Glycogen Synthase Deficiency
    • NCT00694109
      Completed
      Conditions: Lipid Metabolism, Inborn Errors; Hypercholesterolemia, Autosomal Dominant; Hyperlipidemias; Metabolic Diseases; Hyperlipoproteinemia Type II; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Infant, Newborn, Diseases; Metabolic Disorder; Congenital Abnormalities; Hypercholesterolemia; Hyperlipoproteinemias; Dyslipidemias; Lipid Metabolism Disorders
    • NCT00607373
      Completed
      Conditions: Lipid Metabolism, Inborn Errors; Hypercholesterolemia, Autosomal Dominant; Hyperlipidemias; Metabolic Diseases; Hyperlipoproteinemia Type II; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Infant, Newborn, Diseases; Metabolic Disorder; Congenital Abnormalities; Hypercholesterolemia; Hyperlipoproteinemias; Dyslipidemias; Lipid Metabolism Disorders
    • NCT00477594
      Completed
      Conditions: Lipid Metabolism, Inborn Errors; Hypercholesterolemia, Autosomal Dominant; Hyperlipidemias; Metabolic Diseases; Hyperlipoproteinemia Type II; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Infant, Newborn, Diseases; Metabolic Disorder; Congenital Abnormalities; Hypercholesterolemia; Hyperlipoproteinemias; Dyslipidemias; Lipid Metabolism Disorders
    • NCT00362180
      Completed
      Conditions: Lipid Metabolism, Inborn Errors; Hyperlipidemias; Metabolic Diseases; Hypolipoproteinemia; Hypolipoproteinemias; Hypobetalipoproteinemias; Metabolism, Inborn Errors; Genetic Diseases, Inborn; Infant, Newborn, Diseases; Congenital Abnormalities; Metabolic Disorder; Hypercholesterolemia; Dyslipidemias; Lipid Metabolism Disorders
    • NCT03384420
      Enrolling by invitation
      Conditions: Mitochondrial Diseases; Pearson Syndrome
    • NCT02327364
      Completed
      Conditions: Pearson Syndrome
    • NCT02104336
      Terminated
      Conditions: Pearson Syndrome
    • NCT03875105
      Not yet recruiting
      Conditions: Lipid Storage Disease
    • NCT02918032
      Recruiting
      Conditions: Neutral Lipid Storage Disease
    • NCT01527318
      Completed
      Conditions: Neutral Lipid Storage Disease
    • NCT02830763
      Terminated
      Conditions: Primary Triglyceride Deposit Cardiomyovasculopathy (TGCV); Neutral Lipid Storage Disease With Myopathy (NLSD-M)