drugset / Trial / NCT01336608
A 24-week Arterial Stiffness Study With Fluticasone Furoate/Vilanterol in COPD
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of the study is to investigate the effect of fluticasone furoate/vilanterol Inhalation Powder on arterial stiffness compared with placebo and vilanterol over a 24-week treatment period in subjects with COPD and aortic pulse wave velocity of 11.0 m/s or above.
Timeline
- Start
- 2011-03-04
- Primary completion
- 2014-11-04
- Completion
- 2014-11-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Fluticasone Furoate | Other / unclassified | 100 ug | Other |
| Subject | Vilanterol | Other / unclassified | 25 ug | Other |