CLINICAL_TRIALS ClinicalTrials.gov record update

Randomised, Double-blind, Double-dummy, Placebo-controlled, 4-way Cross-over Study to Characterise the 24-hour FEV1-time Profiles of BI 1744 CL 5μg and 10μg (Oral Inhalation, Delivered by the Respimat® Inhaler) and Tiotropium Bromide 18μg (Oral Inhalation, Delivered by the HandiHaler®) After 6 Weeks of Treatment in Patients With Chronic Obstructive Pulmonary Disease (COPD)

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT01040728
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:35:40.232103+00:00
Published At: 2014-06-30T00:00:00+00:00
Record Updated At: 2014-06-30
Results Posted At: 2014-06-30
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["Pulmonary Disease, Chronic Obstructive"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2014-06-30"
protocolSection.identificationModule.nctId: "NCT01040728"
protocolSection.identificationModule.officialTitle: "Randomised, Double-blind, Double-dummy, Placebo-controlled, 4-way Cross-over Study to Characterise the 24-hour FEV1-time Profiles of BI 1744 CL 5\u03bcg and 10\u03bcg (Oral Inhalation, Delivered by the Respimat\u00ae Inhaler) and Tiotropium Bromide 18\u03bcg (Oral Inhalation, Delivered by the HandiHaler\u00ae) After 6 Weeks of Treatment in Patients With Chronic Obstructive Pulmonary Disease (COPD)"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: "2014-06-30"

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