CLINICAL_TRIALS
ClinicalTrials.gov record update
A Patient Registry and Natural History Study of Patients with Biallelic HPDL Mutations
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
- NCT05848271
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-25T22:26:40.849028+00:00
- Published At
- 2025-03-30T00:00:00+00:00
- Record Updated At
- 2025-03-30
- 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
["Mitochondrial Encephalomyopathies", "Hereditary Spastic Paraplegia", "Spastic Paraplegia", "White Matter Disease", "Neonatal Encephalopathy", "Mutation", "Genetic Disease"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-03-30"- protocolSection.identificationModule.nctId
"NCT05848271"- protocolSection.identificationModule.officialTitle
"A Patient Registry and Natural History Study of Patients with Biallelic HPDL Mutations"- protocolSection.statusModule.overallStatus
"RECRUITING"- 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.