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CLINICAL_TRIALS ClinicalTrials.gov record update

Whole Genome Analysis for the Detection of Key Genes in the Polycystic Ovary Syndrome - a Study on Multigenerational Families

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
NCT00665171
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:34:55.515877+00:00
Published At
2008-04-23T00:00:00+00:00
Record Updated At
2008-04-23
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
["Anovulation", "Hyperandrogenism", "Polycystic Ovary Syndrome", "Single Nucleotide Polymorphism"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2008-04-23"
protocolSection.identificationModule.nctId
"NCT00665171"
protocolSection.identificationModule.officialTitle
"Whole Genome Analysis for the Detection of Key Genes in the Polycystic Ovary Syndrome - a Study on Multigenerational Families"
protocolSection.statusModule.overallStatus
"UNKNOWN"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Anovulation (protocolSection.conditionsModule.conditions)
  • Hyperandrogenism (protocolSection.conditionsModule.conditions)
  • Polycystic Ovary Syndrome (protocolSection.conditionsModule.conditions)
  • Single Nucleotide Polymorphism (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.