drugset / Trial / NCT00668772
Tiotropium/Salmeterol Inhalation Powder in COPD
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Salmeterol | Other / unclassified | 25 ug | Oral |
| Subject | Tiotropium | Other / unclassified | 7.5 ug | Oral |
| Subject | Tiotropium | Other / unclassified | 18 ug | Oral |