CLINICAL_TRIALS
ClinicalTrials.gov record update
Dietary Therapy for Inherited Disorders of Energy Metabolism
This page presents selected fields from the linked source record. It does not add a medical interpretation.
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
Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.
This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.