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A multicentre, randomised, double-blind, parallel group, placebo-controlled study to investigate the long-term effects of salmeterol/fluticasone propionate (SERETIDE® inhaler) 50/500mcg BD, salmeterol 50mcg BD and fluticasone propionate 500mcg BD, all delivered via the DISKUS®/ACCUHALER® inhaler, on mortality and morbidity of subjects with chronic obstructive pulmonary disease (COPD) over 3 years of treatment |
fluticasone propionate/salmeterol |
SCO30003 |
NCT00268216 |
Pulmonary Disease, Chronic Obstructive |
Phase 3 |
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An analysis-ready dataset is not available for this study. |
September 2013 |