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CLINICAL_TRIALS ClinicalTrials.gov record update

Testing of NBIA Genes: Analysis of Genetic Heterogeneity and Validation of Mitochondrial Markers for Assessing Causality of Sequence Variants.

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT05615571
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:38:54.557432+00:00
Published At
2022-11-14T00:00:00+00:00
Record Updated At
2022-11-14
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
["Neurodegeneration With Brain Iron Accumulation (NBIA)"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2022-11-14"
protocolSection.identificationModule.nctId
"NCT05615571"
protocolSection.identificationModule.officialTitle
"Testing of NBIA Genes: Analysis of Genetic Heterogeneity and Validation of Mitochondrial Markers for Assessing Causality of Sequence Variants."
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Neurodegeneration With Brain Iron Accumulation (NBIA) (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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