Clinical Trials on Glycogen Storage Disease Type V

Total 15 results

    • NCT02432768
      Completed
      Conditions: Glycogen Storage Disease Type V
    • NCT03844022
      Recruiting
      Conditions: Glycogen Storage Disease Type V
    • NCT02919631
      Unknown status
      Conditions: Glycogen Storage Disease Type V
    • NCT03112889
      Completed
      Conditions: Glycogen Storage Disease Type V; McArdle Disease
    • NCT04226274
      Recruiting
      Conditions: McArdle Disease
    • NCT03945370
      Completed
      Conditions: McArdle Disease
    • NCT04044508
      Recruiting
      Conditions: McArdle Disease
    • NCT03843606
      Completed
      Conditions: McArdle Disease
    • NCT04694547
      Not yet recruiting
      Conditions: McArdle Disease
    • NCT04292938
      Recruiting
      Conditions: Glycogen Storage Disease
    • NCT04349566
      Enrolling by invitation
      Conditions: Becker Muscular Dystrophy; McArdle Disease; Limb-Girdle Muscular Dystrophy Type 2
    • NCT03211923
      Unknown status
      Conditions: Nemaline Myopathy Type 6; Myotonic Dystrophy Type 2; McArdle Disease
    • 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
    • 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
    • NCT00674843
      Unknown status
      Conditions: Muscular Dystrophies