Glycogen Storage Disease Type Ix: Clinical Trials

1 trial for Glycogen Storage Disease Type Ix, newest first

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1 unknown. 1 Not applicable.

By phase and status

PhaseTrialsStatus
Not applicable1Unknown 1

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TrialPhaseStatusSponsorEnrollmentStartUpdated
Fat and Sugar Metabolism During Exercise in Patients With Metabolic Myopathy
Sugar - Metabolism, Inborn Errors, Lipid Metabolism, Inborn Errors
Not applicableUnknownCopenhagen University Hospital, Rigshospitalet602016-01-012019-10-16

Narrower conditions

Carbohydrate Metabolism, Inborn Errors (1)  ·  Carnitine palmitoyl transferase 2 deficiency (1)  ·  Chanarin-Dorfman Syndrome (1)  ·  Dimauro disease (1)  ·  Glycogen Storage Disease Type II (1)  ·  Glycogen Storage Disease Type III (1)  ·  Glycogen Storage Disease Type IV (1)  ·  Glycogen Storage Disease Type V (1)  ·  Glycogen Storage Disease Type VII (1)  ·  Glycogen Storage Disease XIII (1)  ·  Glycogen Storage Disease XIV (1)  ·  Lactate Dehydrogenase Deficiency (1)  ·  Lipid Metabolism, Inborn Errors (1)  ·  Medium chain acyl CoA dehydrogenase deficiency (1)

Broader conditions

Amino Acid Metabolism, Inborn Errors (1)  ·  Brain Diseases (1)  ·  Brain Diseases, Metabolic (1)  ·  Brain Diseases, Metabolic, Inborn (1)  ·  Central Nervous System Diseases (1)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (1)  ·  Genetic Diseases, Inborn (1)  ·  Glycogen Storage Disease (1)  ·  Lipid Metabolism Disorders (1)  ·  Lysosomal Storage Diseases (1)  ·  Lysosomal Storage Diseases, Nervous System (1)  ·  Metabolic Diseases (1)  ·  Mitochondrial Diseases (1)  ·  Muscular Diseases (1)  ·  Muscular Disorders, Atrophic (1)

Interventions

Sugars (1)

Sponsors

Copenhagen University Hospital, Rigshospitalet (1)

Countries

Denmark (1)

Top investigators

Karen L Madsen, MD (1)

Results publications

PMID 30990523, PMID 31492716