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CLINICAL_TRIALS ClinicalTrials.gov record update

Study of the Efficacy of Propranolol for the Management of Epistaxis in Hereditary Hemorrhagic Telangiectasia Patients

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
NCT04113187
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:38:36.904117+00:00
Published At
2022-06-14T00:00:00+00:00
Record Updated At
2022-06-14
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
["Hereditary Hemorrhagic Telangiectasia", "Osler Weber Rendu Disease"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2022-06-14"
protocolSection.identificationModule.nctId
"NCT04113187"
protocolSection.identificationModule.officialTitle
"Study of the Efficacy of Propranolol for the Management of Epistaxis in Hereditary Hemorrhagic Telangiectasia Patients"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

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