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CLINICAL_TRIALS ClinicalTrials.gov record update

A Randomised, Double-blind, Parallel Group Study to Assess the Efficacy and Safety of 52 Weeks of Once Daily Treatment of Orally Inhaled Tiotropium + Olodaterol Fixed Dose Combination (2.5 µg / 5 µg; 5 µg / 5 µg) (Delivered by the Respimat® Inhaler) Compared With the Individual Components (2.5 µg and 5 µg Tiotropium, 5 µg Olodaterol) (Delivered by the Respimat® Inhaler) in Patients With Chronic Obstructive Pulmonary Disease (COPD). [TOnado TM 1]

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01431274
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:35:52.594924+00:00
Published At
2015-07-16T00:00:00+00:00
Record Updated At
2015-07-16
Results Posted At
2015-07-16
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
["Pulmonary Disease, Chronic Obstructive"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2015-07-16"
protocolSection.identificationModule.nctId
"NCT01431274"
protocolSection.identificationModule.officialTitle
"A Randomised, Double-blind, Parallel Group Study to Assess the Efficacy and Safety of 52 Weeks of Once Daily Treatment of Orally Inhaled Tiotropium + Olodaterol Fixed Dose Combination (2.5 \u00b5g / 5 \u00b5g; 5 \u00b5g / 5 \u00b5g) (Delivered by the Respimat\u00ae Inhaler) Compared With the Individual Components (2.5 \u00b5g and 5 \u00b5g Tiotropium, 5 \u00b5g Olodaterol) (Delivered by the Respimat\u00ae Inhaler) in Patients With Chronic Obstructive Pulmonary Disease (COPD). [TOnado TM 1]"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2015-07-16"

Study condition terms

  • Pulmonary Disease, Chronic Obstructive (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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