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CLINICAL_TRIALS ClinicalTrials.gov record update

Human Epilepsy Genetics--Neuronal Migration Disorders Study

This page presents selected fields from the linked source record. It does not add a medical interpretation.

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT00041600
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:39:34.704348+00:00
Published At
2023-09-21T00:00:00+00:00
Record Updated At
2023-09-21
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
["Brain Malformation", "Neuronal Migration Disorder", "Cognition Disorder", "Epilepsy"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2023-09-21"
protocolSection.identificationModule.nctId
"NCT00041600"
protocolSection.identificationModule.officialTitle
"Human Epilepsy Genetics--Neuronal Migration Disorders Study"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Brain Malformation (protocolSection.conditionsModule.conditions)
  • Neuronal Migration Disorder (protocolSection.conditionsModule.conditions)
  • Cognition Disorder (protocolSection.conditionsModule.conditions)
  • Epilepsy (protocolSection.conditionsModule.conditions)

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.