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CLINICAL_TRIALS ClinicalTrials.gov record update

Natural History Study of Individuals With Autism and Germline Heterozygous PTEN Mutations

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
NCT02461446
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:27:10.560136+00:00
Published At
2024-10-26T00:00:00+00:00
Record Updated At
2024-10-26
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
["PTEN", "ASD", "Autism", "Macrocephaly", "PTEN Hamartoma Tumor Syndrome"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2024-10-26"
protocolSection.identificationModule.nctId
"NCT02461446"
protocolSection.identificationModule.officialTitle
"Natural History Study of Individuals With Autism and Germline Heterozygous PTEN Mutations"
protocolSection.statusModule.overallStatus
"RECRUITING"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • PTEN (protocolSection.conditionsModule.conditions)
  • ASD (protocolSection.conditionsModule.conditions)
  • Autism (protocolSection.conditionsModule.conditions)
  • Macrocephaly (protocolSection.conditionsModule.conditions)
  • PTEN Hamartoma Tumor 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.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.