|Clinical Study ID||
|Study Title||A randomized, double-blind, placebo-controlled, parallel-group, trial evaluating the safety and efficacy of the Diskus formulation of salmeterol 50mcg twice daily and fluticasone propionate 250mcg twice daily individually and in combination as compared to placebo in COPD patients.|
|Patient Level Data||Study Listed on ClinicalStudyDataRequest.com|
|Study Recruitment Status||Completed|
|Generic Name||fluticasone propionate/salmeterol|
|Trade Name||advair; seretide|
|Study Indication||Pulmonary Disease, Chronic Obstructive|
For more information on this register please email GSKClinicalSupportHD@gsk.com
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