|Clinical Study ID||
|Study Title||A multicentre, randomised, double-blind, parallel group study to compare the efficacy and safety of the Salmeterol/Fluticasone combination product (50/500mg strength) twice daily with Salmeterol 50mg twice daily alone and Fluticasone Propionate 500mg twice daily alone, all delivered via the Diskus/Accuhaler inhaler, in the treatment of patients with chronic obstructive pulmonary disease.|
|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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