Clinical Trials on Primary Carnitine Deficiency

Total 8 results

    • NCT01904396
      Unknown status
      Conditions: Carnitine Deficiency
    • NCT00187733
      Completed
      Conditions: Carnitine Transporter Deficiency
    • NCT02226419
      Completed
      Conditions: Carnitine Transporter, Plasma-membrane, Deficiency of
    • NCT01783041
      Active, not recruiting
      Conditions: Prematurity; Neurodevelopmental Disorder; Carnitine Deficiency
    • NCT00351234
      Completed
      Conditions: Diabetes Mellitus, Type I; Hypoglycemia
    • 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
    • NCT00079599
      Completed
      Conditions: HIV Infections; AIDS
    • NCT00091169
      Completed
      Conditions: Fatigue; Unspecified Adult Solid Tumor, Protocol Specific