Clinical trial

Bone Mineral Density Study In Patients With Chronic Obstructive Pulmonary…

NCT00355342 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00355342
Title Bone Mineral Density Study In Patients With Chronic Obstructive Pulmonary Disease. DISKUS® Inhaler is a Trademark of the GSK Group of Companies.
Official title A Randomized, Double-Blind, Parallel-Group Clinical Trial Evaluating the Effect of the Fluticasone Propionate/Salmeterol Combination Product 250/50mcg Twice Daily Via DISKUS® Inhaler Versus Salmeterol 50mcg Twice Daily Via DISKUS® Inhaler on Bone Mineral Density in Subjects With Chronic Obstructive…
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Pulmonary Disease, Chronic Obstructive
Intervention type Device, Drug
Interventions Salmeterol 50 mcg BID, Fluticasone Propionate/Salmeterol 250/50 mcg BID, DISKUS inhaler
Enrollment 186
Start date Apr 28, 2004
Primary completion Sep 6, 2007
Completion Sep 6, 2007
First posted Jul 21, 2006
Last update posted Jul 2, 2018
Countries 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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