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Completed Phase 4 Interventional Results available

A Study Measuring Asthma Control In Pediatric And Adolescent Subjects Whose Asthma Is Worsened By Activity Or Exercise

ClinicalTrials.gov ID: NCT00118716

Public ClinicalTrials.gov record NCT00118716. 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, 2:12 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 Stratified, Multicenter, Randomized, Double-Blind, Parallel Group, 4-Week Comparison of Fluticasone Propionate/Salmeterol DISKUS Combination Product 100/50mcg BID Versus Fluticasone Propionate DISKUS 100mcg BID in Pediatric and Adolescent Subjects With Activity-Induced Bronchospasm

Brief summary

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

During this study, your child will need to attend up to 5 office visits and maintain regular telephone contact with the clinic. Certain office visits will include physical exams, medical history review, exercise challenge test (walking/running on a treadmill), electrocardiogram (ECG) tests, and lung function tests. All study related medications and medical examinations are provided at no cost. All study drugs are currently available by prescription to patients 4 years and older.

Study identification

NCT ID
NCT00118716
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
248 participants

Conditions and interventions

Eligibility (public fields only)

Age range
4 Years to 17 Years
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 23, 2003 (Actual)
Primary completion
Apr 1, 2006 (Actual)
Completion
Apr 23, 2006 (Actual)
Last update posted
Feb 5, 2019

2003 – 2006

United States locations

U.S. sites
50
U.S. states
22
U.S. cities
48
Facility City State ZIP Site status
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Huntington Beach California 92647 —
GSK Investigational Site Orange California 92868 —
GSK Investigational Site Palmdale California 93551 —
GSK Investigational Site Paramount California 90723 —
GSK Investigational Site San Diego California 92120 —
GSK Investigational Site Torrance California 90503 —
GSK Investigational Site Walnut Creek California 94598 —
GSK Investigational Site Centennial Colorado 80112 —
GSK Investigational Site Englewood Colorado 80112 —
GSK Investigational Site Lakewood Colorado 80401 —
GSK Investigational Site Miami Florida 33156 —
GSK Investigational Site Miami Florida 33176 —
GSK Investigational Site Tallahassee Florida 32308 —
GSK Investigational Site Lilburn Georgia 30047 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Hoffman Estates Illinois 60195 —
GSK Investigational Site Metairie Louisiana 70001 —
GSK Investigational Site Metairie Louisiana 70006 —
GSK Investigational Site Baltimore Maryland 21236 —
GSK Investigational Site Glen Burnie Maryland 21061 —
GSK Investigational Site North Dartmouth Massachusetts 02747 —
GSK Investigational Site Minneapolis Minnesota 55402 —
GSK Investigational Site Papillion Nebraska 68046 —
GSK Investigational Site Skillman New Jersey 08558 —
GSK Investigational Site Summit New Jersey 07901 —
GSK Investigational Site Commack New York 11725 —
GSK Investigational Site Utica New York 13502 —
GSK Investigational Site Canton Ohio 44718 —
GSK Investigational Site Cincinnati Ohio 45231 —
GSK Investigational Site Dayton Ohio 45404 —
GSK Investigational Site Gresham Oregon 97030 —
GSK Investigational Site Medford Oregon 97504 —
GSK Investigational Site Portland Oregon 97213 —
GSK Investigational Site Erie Pennsylvania 16508 —
GSK Investigational Site Hershey Pennsylvania 17033-0850 —
GSK Investigational Site Philadelphia Pennsylvania 19135 —
GSK Investigational Site Pittsburgh Pennsylvania 15212 —
GSK Investigational Site Charleston South Carolina 29406 —
GSK Investigational Site Mt. Pleasant South Carolina 29464 —
GSK Investigational Site Orangeburg South Carolina 29118 —
GSK Investigational Site Dyersburg Tennessee 38024 —
GSK Investigational Site Knoxville Tennessee 37922 —
GSK Investigational Site Dallas Texas 75204 —
GSK Investigational Site Houston Texas 77074 —
GSK Investigational Site Murray Utah 84107 —
GSK Investigational Site Richmond Virginia 23298 —
GSK Investigational Site Greenfield Wisconsin 53228 —
GSK Investigational Site Madison Wisconsin 53792 —
GSK Investigational Site Milwaukee Wisconsin 53226 —

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 NCT00118716, 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 Feb 5, 2019 · Synced Oct 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 public registry record, listed eligibility criteria, and available contact information for NCT00118716 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →