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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 Oct 18, 2026, 2:10 AM 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
Oct 2004 (Type not available)
Primary completion
Dec 2006 (Actual)
Completion
Dec 2006 (Actual)
Last update posted
Oct 28, 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 28, 2016 · Synced Oct 18, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00144911 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →