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Completed Phase 4 Interventional Results available

Bone Mineral Density Study In Patients With Chronic Obstructive Pulmonary Disease. DISKUS® Inhaler is a Trademark of the GSK Group of Companies.

ClinicalTrials.gov ID: NCT00355342

Public ClinicalTrials.gov record NCT00355342. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 6:19 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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 Pulmonary Disease (COPD)

Study identification

NCT ID
NCT00355342
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
186 participants

Conditions and interventions

Interventions

  • Salmeterol 50 mcg BID Drug
  • Fluticasone Propionate/Salmeterol 250/50 mcg BID Drug
  • DISKUS inhaler Device

Drug · Device

Eligibility (public fields only)

Age range
40 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 27, 2004
Primary completion
Sep 5, 2007
Completion
Sep 5, 2007
Last update posted
Jul 1, 2018

2004 – 2007

United States locations

U.S. sites
37
U.S. states
19
U.S. cities
34
Facility City State ZIP Site status
GSK Investigational Site Berkeley California 94705
GSK Investigational Site Fullerton California 92835
GSK Investigational Site Rancho Mirage California 92270
GSK Investigational Site San Diego California 92103
GSK Investigational Site Walnut Creek California 94598
GSK Investigational Site Fort Collins Colorado 80528
GSK Investigational Site Wheat Ridge Colorado 80033
GSK Investigational Site Hartford Connecticut 06105
GSK Investigational Site Fort Lauderdale Florida 33316
GSK Investigational Site Jacksonville Florida 32205
GSK Investigational Site Sarasota Florida 34239
GSK Investigational Site Tamarac Florida 33321
GSK Investigational Site Atlanta Georgia 30342
GSK Investigational Site Chicago Illinois 60612
GSK Investigational Site North Chicago Illinois 60064
GSK Investigational Site Wichita Kansas 67207
GSK Investigational Site Boston Massachusetts 02135
GSK Investigational Site Cadillac Michigan 49601
GSK Investigational Site Saint Charles Missouri 63301
GSK Investigational Site Omaha Nebraska 68124
GSK Investigational Site Bronxville New York 10708
GSK Investigational Site Charlotte North Carolina 28207
GSK Investigational Site Portland Oregon 97213
GSK Investigational Site Charleston South Carolina 29406-7108
GSK Investigational Site Greer South Carolina 29651
GSK Investigational Site Simpsonville South Carolina 29681
GSK Investigational Site Spartanburg South Carolina 29303
GSK Investigational Site Kingsport Tennessee 37660
GSK Investigational Site Milan Tennessee 38372
GSK Investigational Site Corsicana Texas 75110
GSK Investigational Site San Antonio Texas 78205
GSK Investigational Site San Antonio Texas 78217
GSK Investigational Site Richmond Virginia 23225
GSK Investigational Site Richmond Virginia 23249
GSK Investigational Site Bellingham Washington 98226
GSK Investigational Site Spokane Washington 99202
GSK Investigational Site Spokane Washington 99204

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00355342, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 1, 2018 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00355342 live on ClinicalTrials.gov.

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