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A Randomised, Double Blind, Placebo Controlled, 4 Period, Incomplete Block, Crossover Study to Assess the Dose-response Curve of Intranasal Fluticasone Propionate (25, 50, 100 and 200 μg, Once Daily for 8 Days) in the Vienna Challenge Chamber for the Purpose of Investigating the Sensitivity

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT00848965
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:35:16.255534+00:00
Published At
2012-09-24T00:00:00+00:00
Record Updated At
2012-09-24
Results Posted At
2012-09-24
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
["Rhinitis, Allergic, Perennial", "Allergic Rhinitis"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2012-09-24"
protocolSection.identificationModule.nctId
"NCT00848965"
protocolSection.identificationModule.officialTitle
"A Randomised, Double Blind, Placebo Controlled, 4 Period, Incomplete Block, Crossover Study to Assess the Dose-response Curve of Intranasal Fluticasone Propionate (25, 50, 100 and 200 \u03bcg, Once Daily for 8 Days) in the Vienna Challenge Chamber for the Purpose of Investigating the Sensitivity"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE4"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2012-09-24"

Study condition terms

  • Rhinitis, Allergic, Perennial (protocolSection.conditionsModule.conditions)
  • Allergic Rhinitis (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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