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CLINICAL_TRIALS ClinicalTrials.gov record update

Dietary Therapy for Inherited Disorders of Energy Metabolism

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01461304
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:38:22.294961+00:00
Published At
2021-12-10T00:00:00+00:00
Record Updated At
2021-12-10
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
["Very Long-chain acylCoA Dehydrogenase (VLCAD) Deficiency", "Carnitine Palmitoyltransferase Deficiencies (CPT1, CPT2)", "Mitochondrial Trifunctional Protein Deficiency", "Long-chain Hydroxyacyl-CoA Dehydrogenase Deficiency", "Glycogen Storage Disorders", "Pyruvate Carboxylase Deficiency Disease", "ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 9, DEFICIENCY of", "Barth Syndrome"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2021-12-10"
protocolSection.identificationModule.nctId
"NCT01461304"
protocolSection.identificationModule.officialTitle
"Dietary Therapy for Inherited Disorders of Energy Metabolism"
protocolSection.statusModule.overallStatus
"NO_LONGER_AVAILABLE"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Very Long-chain acylCoA Dehydrogenase (VLCAD) Deficiency (protocolSection.conditionsModule.conditions)
  • Carnitine Palmitoyltransferase Deficiencies (CPT1, CPT2) (protocolSection.conditionsModule.conditions)
  • Mitochondrial Trifunctional Protein Deficiency (protocolSection.conditionsModule.conditions)
  • Long-chain Hydroxyacyl-CoA Dehydrogenase Deficiency (protocolSection.conditionsModule.conditions)
  • Glycogen Storage Disorders (protocolSection.conditionsModule.conditions)
  • Pyruvate Carboxylase Deficiency Disease (protocolSection.conditionsModule.conditions)
  • ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 9, DEFICIENCY of (protocolSection.conditionsModule.conditions)
  • Barth Syndrome (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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