Clinical Trials on Glycogen Storage Disease Type V

Total 6 results

  • NCT02385162
    Active, not recruiting
    Conditions: Fructose Metabolism, Inborn Errors, Glycogen Storage Disease, Glycogen Storage Disease Type I, Glycogen Storage Disease Type II, Glycogen Storage Disease Type III, Glycogen Storage Disease Type IV, Glycogen Storage Disease Type V, Glycogen Storage Disease Type VI, Glycogen Storage Disease Type VII, Glycogen Storage Disease Type VIII
  • NCT03844022
    Recruiting
    Conditions: Glycogen Storage Disease Type V
  • 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
  • NCT02432768
    Completed
    Conditions: Glycogen Storage Disease Type V
  • NCT03112889
    Completed
    Conditions: Glycogen Storage Disease Type V, McArdle Disease
  • NCT02919631
    Unknown status
    Conditions: Glycogen Storage Disease Type V