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Completed Phase 4 Interventional Results available

Validation of a New Shortness of Breath With Daily Activities Questionnaire in Patients With Chronic Obstructive Pulmonary Disease

ClinicalTrials.gov ID: NCT00984659

Public ClinicalTrials.gov record NCT00984659. 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 22, 2026, 8:43 AM EDT

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

Study identification

NCT ID
NCT00984659
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
366 participants

Conditions and interventions

Interventions

  • Fluticasone propionate/salmeterol combination product Drug
  • Salmeterol Drug
  • Placebo Drug

Drug

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 28, 2009
Primary completion
Jun 30, 2010
Completion
Jun 30, 2010
Last update posted
Aug 28, 2018

2009 – 2010

United States locations

U.S. sites
39
U.S. states
20
U.S. cities
38
Facility City State ZIP Site status
GSK Investigational Site Jasper Alabama 35501
GSK Investigational Site Mobile Alabama 36608
GSK Investigational Site Los Angeles California 90095-1690
GSK Investigational Site Riverside California 92506
GSK Investigational Site Wheat Ridge Colorado 80033
GSK Investigational Site Stamford Connecticut 06902
GSK Investigational Site Tamarac Florida 33321
GSK Investigational Site Decatur Georgia 30033
GSK Investigational Site Lawrenceville Georgia 30046
GSK Investigational Site Evansville Indiana 47710
GSK Investigational Site Evansville Indiana 47714
GSK Investigational Site South Bend Indiana 46617
GSK Investigational Site Madisonville Kentucky 42431
GSK Investigational Site New Orleans Louisiana 70115
GSK Investigational Site Sunset Louisiana 70584
GSK Investigational Site St Louis Missouri 63141
GSK Investigational Site Summit New Jersey 07091
GSK Investigational Site Charlotte North Carolina 28207
GSK Investigational Site Elizabeth City North Carolina 27909
GSK Investigational Site Canton Ohio 44718
GSK Investigational Site Cincinnati Ohio 45231
GSK Investigational Site Lake Oswego Oregon 97035
GSK Investigational Site Portland Oregon 97213
GSK Investigational Site Erie Pennsylvania 16508
GSK Investigational Site Philadelphia Pennsylvania 19140
GSK Investigational Site Charleston South Carolina 29406-7108
GSK Investigational Site Chester South Carolina 29706
GSK Investigational Site Clinton South Carolina 29325
GSK Investigational Site Easley South Carolina 29640
GSK Investigational Site Gaffney South Carolina 29340
GSK Investigational Site Greenwood South Carolina 29646
GSK Investigational Site Seneca South Carolina 29678
GSK Investigational Site Spartanburg South Carolina 29303
GSK Investigational Site Johnson City Tennessee 37601
GSK Investigational Site Houston Texas 77054
GSK Investigational Site New Braunfels Texas 78130
GSK Investigational Site Abingdon Virginia 24210
GSK Investigational Site Richmond Virginia 23229
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 NCT00984659, 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 Aug 28, 2018 · Synced Jul 22, 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 protocol, eligibility criteria, and contact information for NCT00984659 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →