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ClinicalTrials.gov record
Completed Phase 4 Interventional

Advair® DISKUS® Versus Serevent® DISKUS® For Chronic Obstructive Pulmonary Disease Exacerbations

ClinicalTrials.gov ID: NCT00115492

Public ClinicalTrials.gov record NCT00115492. 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 22, 2026, 6:47 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 Combination Product 250/50mcg BID With Salmeterol Diskus 50mcg BID on the Annual Rate of Moderate/Severe Exacerbations in Subjects With Chronic Obstructive Pulmonary Disease

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 FDA for use in patients with COPD.

Study identification

NCT ID
NCT00115492
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
797 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
Dec 2004 (Type not available)
Primary completion
Jun 2007 (Actual)
Completion
Jun 2007 (Actual)
Last update posted
Jan 20, 2017

2004 – 2007

United States locations

U.S. sites
95
U.S. states
35
U.S. cities
91
Facility City State ZIP Site status
GSK Investigational Site Jasper Alabama 35501 —
GSK Investigational Site Mobile Alabama 36608 —
GSK Investigational Site Glendale Arizona 85306 —
GSK Investigational Site Phoenix Arizona 85013 —
GSK Investigational Site Berkeley California 94705 —
GSK Investigational Site Fullerton California 92835 —
GSK Investigational Site Riverside California 92506 —
GSK Investigational Site Sacramento California 95825 —
GSK Investigational Site San Diego California 92123 —
GSK Investigational Site Vista California 92084 —
GSK Investigational Site Fort Collins Colorado 80528 —
GSK Investigational Site Stamford Connecticut 06902 —
GSK Investigational Site Atlantis Florida 33462 —
GSK Investigational Site Clearwater Florida 33756 —
GSK Investigational Site DeLand Florida 32720 —
GSK Investigational Site Fort Lauderdale Florida 33316 —
GSK Investigational Site Pensacola Florida 32504 —
GSK Investigational Site Sarasota Florida 34239 —
GSK Investigational Site Tamarac Florida 33321 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Woodstock Georgia 30189 —
GSK Investigational Site Springfield Illinois 62702 —
GSK Investigational Site Elkhart Indiana 46154 —
GSK Investigational Site Evansville Indiana 47710 —
GSK Investigational Site Evansville Indiana 47714 —
GSK Investigational Site Indianapolis Indiana 46208 —
GSK Investigational Site South Bend Indiana 46617 —
GSK Investigational Site Iowa City Iowa 52242 —
GSK Investigational Site Olathe Kansas 66061 —
GSK Investigational Site Madisonville Kentucky 42431 —
GSK Investigational Site Lafayette Louisiana 70503 —
GSK Investigational Site New Orleans Louisiana 70112 —
GSK Investigational Site Shreveport Louisiana 71103 —
GSK Investigational Site Sunset Louisiana 70584 —
GSK Investigational Site Auburn Maine 04210 —
GSK Investigational Site Baltimore Maryland 21201 —
GSK Investigational Site Boston Massachusetts 02135 —
GSK Investigational Site Saint Joseph Michigan 49085 —
GSK Investigational Site Minneapolis Minnesota 55407 —
GSK Investigational Site Chesterfield Missouri 63017 —
GSK Investigational Site Jefferson City Missouri 65101 —
GSK Investigational Site Saint Charles Missouri 63301 —
GSK Investigational Site St Louis Missouri 63110 —
GSK Investigational Site Billings Montana 59102 —
GSK Investigational Site Butte Montana 59701 —
GSK Investigational Site Omaha Nebraska 68124 —
GSK Investigational Site Omaha Nebraska 68131 —
GSK Investigational Site Absecon New Jersey 08201 —
GSK Investigational Site Albany New York 12205 —
GSK Investigational Site Bay Shore New York 11706 —
GSK Investigational Site Ithaca New York 14850 —
GSK Investigational Site Larchmont New York 10538 —
GSK Investigational Site New York New York 10016 —
GSK Investigational Site Chapel Hill North Carolina 27599 —
GSK Investigational Site Charlotte North Carolina 28207 —
GSK Investigational Site Elizabeth City North Carolina 27909 —
GSK Investigational Site High Point North Carolina 27262 —
GSK Investigational Site Raleigh North Carolina 27612 —
GSK Investigational Site Winston-Salem North Carolina 27157 —
GSK Investigational Site Canton Ohio 44718 —
GSK Investigational Site Chardon Ohio 44024 —
GSK Investigational Site Mogadore Ohio 44260 —
GSK Investigational Site Lake Oswego Oregon 97035 —
GSK Investigational Site Erie Pennsylvania 16508 —
GSK Investigational Site Hershey Pennsylvania 17033 —
GSK Investigational Site McKeesport Pennsylvania 15132 —
GSK Investigational Site Pittsburgh Pennsylvania 15025 —
GSK Investigational Site Pittsburgh Pennsylvania 15243 —
GSK Investigational Site East Providence Rhode Island 02914 —
GSK Investigational Site Providence Rhode Island 2909 —
GSK Investigational Site Gaffney South Carolina 29340 —
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 Chattanooga Tennessee 37403 —
GSK Investigational Site Johnson City Tennessee 37601 —
GSK Investigational Site Kingsport Tennessee 37660 —
GSK Investigational Site Dallas Texas 75390-9016 —
GSK Investigational Site Houston Texas 77074 —
GSK Investigational Site New Braunfels Texas 78130 —
GSK Investigational Site San Antonio Texas 78217 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site San Marcos Texas 78666 —
GSK Investigational Site Abingdon Virginia 24210 —
GSK Investigational Site Lynchburg Virginia 24501 —
GSK Investigational Site Newport News Virginia 23606 —
GSK Investigational Site Richmond Virginia 23225 —
GSK Investigational Site Bellingham Washington 98226 —
GSK Investigational Site Gig Harbor Washington 98335 —
GSK Investigational Site Kirkland Washington 98034 —
GSK Investigational Site Spokane Washington 99204 —
GSK Investigational Site Morgantown West Virginia 26505 —
GSK Investigational Site La Crosse Wisconsin 54601 —
GSK Investigational Site Milwaukee Wisconsin 53209 —

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 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00115492, 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 Jan 20, 2017 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00115492 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →