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Genotype-phenotype Association Study of ENG and ACVRL1 Genes in the Inflammatory and Endothelial Response in Hereditary Hemorrhagic Telangiectasia (HHT)

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT05550376
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:26:43.895552+00:00
Published At
2025-03-17T00:00:00+00:00
Record Updated At
2025-03-17
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
["Hereditary Hemorrhagic Telangiectasia", "HHT", "Rendu Osler Weber Disease"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-03-17"
protocolSection.identificationModule.nctId
"NCT05550376"
protocolSection.identificationModule.officialTitle
"Genotype-phenotype Association Study of ENG and ACVRL1 Genes in the Inflammatory and Endothelial Response in Hereditary Hemorrhagic Telangiectasia (HHT)"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Hereditary Hemorrhagic Telangiectasia (protocolSection.conditionsModule.conditions)
  • HHT (protocolSection.conditionsModule.conditions)
  • Rendu Osler Weber Disease (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.