drugset / Trial / NCT00668772

Tiotropium/Salmeterol Inhalation Powder in COPD

NCT00668772

Phase 3 Terminated 207 enrolled Boehringer Ingelheim
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary objectives of this study are to assess bronchodilator efficacy as determined by forced expiratory volume in one second (FEV1), the effect on dyspnoea as determined by the Baseline Dyspnoea Index (BDI)/Transition Dyspnoea Index (TDI), the effect on health status as determined by the St George Respiratory Questionnaire (SGRQ) and the effect on chronic obstructive pulmonary disease (COPD) exacerbations

Timeline

Start
2008-04-15
Primary completion
2008-11-21
Completion
2008-11-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Salmeterol Other / unclassified 25 ug Oral
Subject Tiotropium Other / unclassified 7.5 ug Oral
Subject Tiotropium Other / unclassified 18 ug Oral