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Completed Phase 4 Interventional

ADVAIR® DISKUS® Inhaler (Fluticasone Propionate/Salmeterol) Versus SEREVENT® DISKUS® Inhaler (Salmeterol) For The Treatment Of Chronic Obstructive Pulmonary Disease Exacerbations. ADVAIR® DISKUS® Inhaler and SEREVENT® DISKUS® Inhaler Are Trademarks of the GSK Group of Companies.

ClinicalTrials.gov ID: NCT00144911

Public ClinicalTrials.gov record NCT00144911. 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 Sep 2, 2026, 5:00 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, 52-Week Study to Compare the Effect of Fluticasone Propionate/Salmeterol DISKUS® Inhaler Combination Product 250/50mcg Twice Daily With Salmeterol DISKUS® Inhaler 50mcg Twice Daily on the Annual Rate of Moderate/Severe Exacerbations in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study evaluates the effect of two medicines on COPD (Chronic Obstructive Pulmonary Disease) exacerbations. This study will last up to 56 weeks, and subjects will visit the clinic 10 times. Subjects will be given breathing tests and will record their breathing symptoms daily on diary cards. All study related medicines and medical examinations will be provided at no cost. The two drugs used in this study have been approved by the FDA for use in patients with COPD.

Study identification

NCT ID
NCT00144911
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
740 participants

Conditions and interventions

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
Sep 30, 2004
Primary completion
Nov 30, 2006
Completion
Nov 30, 2006
Last update posted
Oct 27, 2016

2004 – 2006

United States locations

U.S. sites
85
U.S. states
32
U.S. cities
81
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35209
GSK Investigational Site Birmingham Alabama 35294-0012
GSK Investigational Site Jasper Alabama 35501
GSK Investigational Site Glendale Arizona 85306
GSK Investigational Site Phoenix Arizona 85013
GSK Investigational Site Scottsdale Arizona 85258
GSK Investigational Site Little Rock Arkansas 72205
GSK Investigational Site Corona California 92879
GSK Investigational Site Los Angeles California 90095-1752
GSK Investigational Site Palmdale California 93551
GSK Investigational Site Paramount California 90723
GSK Investigational Site Rancho Mirage California 92270
GSK Investigational Site Riverside California 92506
GSK Investigational Site Sacramento California 95825-5480
GSK Investigational Site San Diego California 92120
GSK Investigational Site Sepulveda California 91343
GSK Investigational Site Stockton California 95207
GSK Investigational Site Colorado Springs Colorado 80907
GSK Investigational Site Denver Colorado 80204
GSK Investigational Site Denver Colorado 80206
GSK Investigational Site Englewood Colorado 80113
GSK Investigational Site Wheat Ridge Colorado 80033
GSK Investigational Site DeLand Florida 32720
GSK Investigational Site Jacksonville Florida 32205
GSK Investigational Site Largo Florida 33770
GSK Investigational Site North Miami Beach Florida 33179
GSK Investigational Site Pensacola Florida 32504
GSK Investigational Site Tampa Florida 33613
GSK Investigational Site Coeur d'Alene Idaho 83814
GSK Investigational Site Champaign Illinois 61821
GSK Investigational Site Chicago Illinois 60612
GSK Investigational Site Peoria Illinois 61602
GSK Investigational Site Evansville Indiana 47710
GSK Investigational Site South Bend Indiana 46617
GSK Investigational Site Des Moines Iowa 50309
GSK Investigational Site Lafayette Louisiana 70503
GSK Investigational Site Slidell Louisiana 70458
GSK Investigational Site Auburn Maine 04210
GSK Investigational Site Boston Massachusetts 02118
GSK Investigational Site Worcester Massachusetts 01608
GSK Investigational Site Kalamazoo Michigan 49009
GSK Investigational Site Minneapolis Minnesota 55407
GSK Investigational Site Rochester Minnesota 55905
GSK Investigational Site Kansas City Missouri 64108
GSK Investigational Site Saint Charles Missouri 63301
GSK Investigational Site St Louis Missouri 63122
GSK Investigational Site Omaha Nebraska 68105
GSK Investigational Site Omaha Nebraska 68134
GSK Investigational Site Cherry Hill New Jersey 08003
GSK Investigational Site Summit New Jersey 07091
GSK Investigational Site Albuquerque New Mexico 87108
GSK Investigational Site Larchmont New York 10538
GSK Investigational Site Lewistown New York 14092
GSK Investigational Site Elizabeth City North Carolina 27909
GSK Investigational Site Raleigh North Carolina 27607
GSK Investigational Site Statesville North Carolina 28625
GSK Investigational Site Cincinnati Ohio 45219
GSK Investigational Site Cincinnati Ohio 45231
GSK Investigational Site Cleveland Ohio 44109
GSK Investigational Site Columbus Ohio 43215
GSK Investigational Site Toledo Ohio 43614-5809
GSK Investigational Site Tulsa Oklahoma 74135
GSK Investigational Site Eugene Oregon 97401
GSK Investigational Site Medford Oregon 97504
GSK Investigational Site Portland Oregon 97213
GSK Investigational Site Philadelphia Pennsylvania 19140
GSK Investigational Site Pittsburgh Pennsylvania 15243
GSK Investigational Site Cumberland Rhode Island 02864
GSK Investigational Site Providence Rhode Island 02906
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 Bristol Tennessee 37620
GSK Investigational Site Johnson City Tennessee 37601
GSK Investigational Site Corsicana Texas 75110
GSK Investigational Site Fort Worth Texas 76104
GSK Investigational Site Houston Texas 77030
GSK Investigational Site San Antonio Texas 78229
GSK Investigational Site Abingdon Virginia 24210
GSK Investigational Site Charlottesville Virginia 22908
GSK Investigational Site Newport News Virginia 23606
GSK Investigational Site Gig Harbor Washington 98335
GSK Investigational Site Spokane Washington 99202
GSK Investigational Site Morgantown West Virginia 26505

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00144911, 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 Oct 27, 2016 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00144911 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →