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Completed Phase 4 Interventional Results available

Study Of Allergic Rhinitis In Patients Who Also Have Asthma

ClinicalTrials.gov ID: NCT00296491

Public ClinicalTrials.gov record NCT00296491. 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, 1:18 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 Multicenter, Randomized, Double-Blind, Triple-Dummy, Placebo-Controlled, Parallel Group, Four-Week Study Assessing the Efficacy of Fluticasone Propionate Aqueous Nasal Spray 200mcg QD Versus Montelukast 10mg QD in Adolescent and Adult Subjects With Asthma and Seasonal Allergic Rhinitis Who Are Receiving ADVAIR DISKUS® 100/50mcg BID or Placebo BID

Brief summary

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

This study will last up to 6 weeks. Subjects will visit the clinic up to 5 times. Certain clinic visits will include a physical examination, medical history review, and lung function tests. All study related medications and medical examinations will be provided at no cost to the subject. The drugs used in this study are approved for the age group under study.

Study identification

NCT ID
NCT00296491
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
725 participants

Conditions and interventions

Eligibility (public fields only)

Age range
15 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
Sep 2005 (Type not available)
Primary completion
Oct 2007 (Actual)
Completion
Oct 2007 (Actual)
Last update posted
Dec 16, 2016

2005 – 2007

United States locations

U.S. sites
104
U.S. states
33
U.S. cities
91
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35209 —
GSK Investigational Site Glendale Arizona 85304 —
GSK Investigational Site Scottsdale Arizona 85251 —
GSK Investigational Site Tucson Arizona 85712 —
GSK Investigational Site Hot Springs Arkansas 71913 —
GSK Investigational Site Berkeley California 94705 —
GSK Investigational Site Huntington Beach California 92647 —
GSK Investigational Site Long Beach California 90806 —
GSK Investigational Site Los Angeles California 90025 —
GSK Investigational Site Rancho Mirage California 92270 —
GSK Investigational Site Riverside California 92506 —
GSK Investigational Site Roseville California 95678 —
GSK Investigational Site San Diego California 92103 —
GSK Investigational Site San Diego California 92120 —
GSK Investigational Site San Jose California 95117 —
GSK Investigational Site San Jose California 95128 —
GSK Investigational Site Stockton California 95207 —
GSK Investigational Site Vista California 92083 —
GSK Investigational Site Boulder Colorado 80304 —
GSK Investigational Site Colorado Springs Colorado 80907 —
GSK Investigational Site Fort Collins Colorado 80526 —
GSK Investigational Site Lakewood Colorado 80401 —
GSK Investigational Site Brandon Florida 33511 —
GSK Investigational Site Coral Gables Florida 33134 —
GSK Investigational Site Ocala Florida 34471 —
GSK Investigational Site Pensacola Florida 32504 —
GSK Investigational Site Tallahassee Florida 32308 —
GSK Investigational Site Albany Georgia 31707 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Columbus Georgia 31904 —
GSK Investigational Site Gainesville Georgia 30501 —
GSK Investigational Site Lawrenceville Georgia 30045 —
GSK Investigational Site Savannah Georgia 31405 —
GSK Investigational Site Savannah Georgia 31406 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Springfield Illinois 62704 —
GSK Investigational Site Indianapolis Indiana 46208 —
GSK Investigational Site South Bend Indiana 46617 —
GSK Investigational Site Iowa City Iowa 52242 —
GSK Investigational Site Overland Park Kansas 66210 —
GSK Investigational Site Lexington Kentucky 40536 —
GSK Investigational Site Louisville Kentucky 40215 —
GSK Investigational Site Owensboro Kentucky 42301 —
GSK Investigational Site Baton Rouge Louisiana 70808 —
GSK Investigational Site Covington Louisiana 70433 —
GSK Investigational Site Lafayette Louisiana 70503 —
GSK Investigational Site Shreveport Louisiana 71105 —
GSK Investigational Site Sunset Louisiana 70584 —
GSK Investigational Site Baltimore Maryland 21236 —
GSK Investigational Site North Andover Massachusetts 01845 —
GSK Investigational Site Minneapolis Minnesota 55402 —
GSK Investigational Site Jackson Mississippi 39202 —
GSK Investigational Site Jefferson City Missouri 65101 —
GSK Investigational Site Rolla Missouri 65401 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Warrensburg Missouri 64093 —
GSK Investigational Site Lincoln Nebraska 68505 —
GSK Investigational Site Omaha Nebraska 68124 —
GSK Investigational Site Omaha Nebraska 68130 —
GSK Investigational Site Omaha Nebraska 68131 —
GSK Investigational Site Papillion Nebraska 68046 —
GSK Investigational Site Forked River New Jersey 08731 —
GSK Investigational Site Summit New Jersey 07091 —
GSK Investigational Site Rochester New York 14618 —
GSK Investigational Site Asheville North Carolina 28801 —
GSK Investigational Site Raleigh North Carolina 27607 —
GSK Investigational Site Canton Ohio 44718 —
GSK Investigational Site Cincinnati Ohio 45242 —
GSK Investigational Site Parma Ohio 44129 —
GSK Investigational Site Oklahoma City Oklahoma 73120 —
GSK Investigational Site Bend Oregon 97701 —
GSK Investigational Site Portland Oregon 97213 —
GSK Investigational Site Pittsburgh Pennsylvania 15241 —
GSK Investigational Site Upland Pennsylvania 19013 —
GSK Investigational Site Providence Rhode Island 02906 —
GSK Investigational Site Charleston South Carolina 29407 —
GSK Investigational Site Charleston South Carolina 29414 —
GSK Investigational Site Greenville South Carolina 29607 —
GSK Investigational Site Orangeburg South Carolina 29118 —
GSK Investigational Site Simpsonville South Carolina 29681 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Chattanooga Tennessee 37421 —
GSK Investigational Site Germantown Tennessee 38138 —
GSK Investigational Site Knoxville Tennessee 37909 —
GSK Investigational Site Savannah Tennessee 38372 —
GSK Investigational Site Austin Texas 78750 —
GSK Investigational Site Dallas Texas 75230 —
GSK Investigational Site Dallas Texas 75231-4307 —
GSK Investigational Site Dallas Texas 75240 —
GSK Investigational Site Dallas Texas 75246 —
GSK Investigational Site El Paso Texas 79902 —
GSK Investigational Site El Paso Texas 79925 —
GSK Investigational Site Houston Texas 77054 —
GSK Investigational Site Houston Texas 77070 —
GSK Investigational Site Kerrville Texas 78028 —
GSK Investigational Site San Antonio Texas 78205 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site San Antonio Texas 78233 —
GSK Investigational Site Waco Texas 76708 —
GSK Investigational Site Salt Lake City Utah 84121 —
GSK Investigational Site West Jordan Utah 84084 —
GSK Investigational Site Danville Virginia 24541 —
GSK Investigational Site Richmond Virginia 23298 —
GSK Investigational Site Kirkland Washington 98034 —

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00296491, 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 Dec 16, 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 NCT00296491 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →