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CLINICAL_TRIALS ClinicalTrials.gov record update

Fat and Sugar Metabolism During Exercise in Patients With Metabolic Myopathy

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT02635269
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:37:32.929177+00:00
Published At
2019-10-16T00:00:00+00:00
Record Updated At
2019-10-16
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.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"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2019-10-16"
protocolSection.identificationModule.nctId
"NCT02635269"
protocolSection.identificationModule.officialTitle
"Fat and Sugar Metabolism During Exercise in Patients With Metabolic Myopathy"
protocolSection.statusModule.overallStatus
"UNKNOWN"
protocolSection.designModule.phases
["NA"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Metabolism, Inborn Errors (protocolSection.conditionsModule.conditions)
  • Lipid Metabolism, Inborn Errors (protocolSection.conditionsModule.conditions)
  • Carbohydrate Metabolism, Inborn Errors (protocolSection.conditionsModule.conditions)
  • Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency (protocolSection.conditionsModule.conditions)
  • Glycogenin-1 Deficiency (Glycogen Storage Disease Type XV) (protocolSection.conditionsModule.conditions)
  • Carnitine Palmitoyl Transferase 2 Deficiency (protocolSection.conditionsModule.conditions)
  • VLCAD Deficiency (protocolSection.conditionsModule.conditions)
  • Medium-chain Acyl-CoA Dehydrogenase Deficiency (protocolSection.conditionsModule.conditions)
  • Multiple Acyl-CoA Dehydrogenase Deficiency (protocolSection.conditionsModule.conditions)
  • Carnitine Transporter Deficiency (protocolSection.conditionsModule.conditions)
  • Neutral Lipid Storage Disease (protocolSection.conditionsModule.conditions)
  • Glycogen Storage Disease Type II (protocolSection.conditionsModule.conditions)
  • Glycogen Storage Disease Type III (protocolSection.conditionsModule.conditions)
  • Glycogen Storage Disease Type IV (protocolSection.conditionsModule.conditions)
  • Glycogen Storage Disease Type V (protocolSection.conditionsModule.conditions)
  • Muscle Phosphofructokinase Deficiency (protocolSection.conditionsModule.conditions)
  • Phosphoglucomutase 1 Deficiency (protocolSection.conditionsModule.conditions)
  • Phosphoglycerate Mutase Deficiency (protocolSection.conditionsModule.conditions)
  • Phosphoglycerate Kinase Deficiency (protocolSection.conditionsModule.conditions)
  • Phosphorylase Kinase Deficiency (protocolSection.conditionsModule.conditions)
  • Beta Enolase Deficiency (protocolSection.conditionsModule.conditions)
  • Lactate Dehydrogenase Deficiency (protocolSection.conditionsModule.conditions)
  • Glycogen Synthase Deficiency (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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