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Completed Phase 4 Interventional

GSK BHR Study (Sont)

ClinicalTrials.gov ID: NCT00920543

Public ClinicalTrials.gov record NCT00920543. 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 1, 2026, 5:35 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 Multicenter, Randomized, Double-blind, Parallel Group, 40-week Comparison of Asthma Control Using Bronchial Hyperresponsiveness as an Additional Guide to Long-term Treatment in Adolescents and Adults Receiving Either Fluticasone Propionate/Salmeterol DISKUS Twice Daily or Fluticasone Propionate DISKUS Twice Daily (or Placebo BID if Asymptomatic)

Brief summary

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

The purpose of this study was to determine whether asthma control and reduced bronchial hyperresponsiveness could be achieved and maintained at a lower dose of inhaled corticosteroids with ADVAIR DISKUS twice-daily or FP twice-daily in adult and adolescent subjects with persistent asthma

Study identification

NCT ID
NCT00920543
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
464 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 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
Jan 31, 2003
Primary completion
Sep 30, 2004
Completion
Sep 30, 2004
Last update posted
Aug 31, 2016

2003 – 2004

United States locations

U.S. sites
52
U.S. states
30
U.S. cities
48
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35209
GSK Investigational Site Phoenix Arizona 85006
GSK Investigational Site Tucson Arizona 85712
GSK Investigational Site Carmichael California 95608
GSK Investigational Site Palmdale California 93551
GSK Investigational Site San Diego California 92103
GSK Investigational Site San Diego California 92120
GSK Investigational Site San Diego California 92123
GSK Investigational Site San Jose California 95117
GSK Investigational Site San Jose California 95128
GSK Investigational Site Walnut Creek California 94598
GSK Investigational Site Colorado Springs Colorado 80907
GSK Investigational Site Denver Colorado 80206
GSK Investigational Site Wheat Ridge Colorado 80033
GSK Investigational Site Hartford Connecticut 06106
GSK Investigational Site Trumbull Connecticut 06611
GSK Investigational Site Bay Pines Florida 33744
GSK Investigational Site Gainesville Florida 32610
GSK Investigational Site Sarasota Florida 34233
GSK Investigational Site Chicago Illinois 60637
GSK Investigational Site Normal Illinois 61761
GSK Investigational Site Indianapolis Indiana 46208
GSK Investigational Site Lafayette Indiana 47904
GSK Investigational Site Iowa City Iowa 52242
GSK Investigational Site Louisville Kentucky 40215
GSK Investigational Site New Orleans Louisiana 70119
GSK Investigational Site Baltimore Maryland 21224
GSK Investigational Site Petoskey Michigan 49770
GSK Investigational Site Minneapolis Minnesota 55407
GSK Investigational Site Butte Montana 59701
GSK Investigational Site Papillion Nebraska 68046
GSK Investigational Site Absecon New Jersey 8201
GSK Investigational Site Cherry Hill New Jersey 08003
GSK Investigational Site Rockville Centre New York 11570
GSK Investigational Site Asheville North Carolina 28801
GSK Investigational Site Statesville North Carolina 28625
GSK Investigational Site Canton Ohio 44718
GSK Investigational Site Sylvania Ohio 43560
GSK Investigational Site Toledo Ohio 43617
GSK Investigational Site Oklahoma City Oklahoma 73120
GSK Investigational Site Medford Oregon 97504
GSK Investigational Site Portland Oregon 97213
GSK Investigational Site Tigard Oregon 97223
GSK Investigational Site Pittsburgh Pennsylvania 15213
GSK Investigational Site Pittsburgh Pennsylvania 15241
GSK Investigational Site Lincoln Rhode Island 2865
GSK Investigational Site Charleston South Carolina 29407
GSK Investigational Site Nashville Tennessee 37203-1424
GSK Investigational Site Houston Texas 77090
GSK Investigational Site Charlottesville Virginia 22908
GSK Investigational Site Bellingham Washington 98226
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 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00920543, 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 31, 2016 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00920543 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →