Clinical trial

A 12-Month Study Comparing Fluticasone Propionate/Salmeterol (ADVAIR) DISKUS…

NCT00452699 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00452699
Title A 12-Month Study Comparing Fluticasone Propionate/Salmeterol (ADVAIR) DISKUS Combination Product 250/50mcg BID To Fluticasone Propionate (FLOVENT) DISKUS 250 mcg BID In Symptomatic Subjects With Asthma
Official title A 52-week, Randomized, Double-Blind, Parallel-Group Study of Fluticasone Propionate/Salmeterol DISKUS Combination Product (FSC) 250/50 mcg BID and Fluticasone Propionate (FP) DISKUS 250 mcg BID in Treatment of Subjects With Asthma
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Asthma
Intervention type Drug
Interventions Fluticasone Propionate/salmeterol xinofoate 250/50 mcg BID, Fluticasone propionate 250 mcg BID
Enrollment 621
Start date May 1, 2007
Primary completion May 1, 2009
Completion May 1, 2009
First posted Mar 27, 2007
Last update posted Dec 8, 2016
Countries Argentina, Brazil, Canada, Philippines, United States

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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