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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00296530
Other study ID # ADA103578
Secondary ID
Status Completed
Phase Phase 4
First received February 23, 2006
Last updated October 27, 2016
Start date September 2005
Est. completion date July 2007

Study information

Verified date October 2016
Source GlaxoSmithKline
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

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.


Description:

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


Recruitment information / eligibility

Status Completed
Enrollment 600
Est. completion date July 2007
Est. primary completion date July 2007
Accepts healthy volunteers No
Gender Both
Age group 15 Years and older
Eligibility Inclusion Criteria:

- Have asthma for at least 3 months prior to the study.

- Have been using an allowed pre-study asthma therapy for at least 3 months prior to study.

- Currently have seasonal allergic rhinitis and have had seasonal onset of allergic rhinitis for at least the two previous allergy seasons.

- Have a positive allergy skin test.

Exclusion Criteria:

- Have a history of life-threatening asthma.

- Been hospitalized for asthma within the 6 months prior to the study.

- Have certain conditions that would make study participation unsafe.

The study doctor will evaluate other inclusion and exclusion criteria.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
fluticasone propionate/salmeterol

fluticasone propionate

montelukast


Locations

Country Name City State
United States GSK Investigational Site Austin Texas
United States GSK Investigational Site Austin Texas
United States GSK Investigational Site Baltimore Maryland
United States GSK Investigational Site Bethesda Maryland
United States GSK Investigational Site Charleston South Carolina
United States GSK Investigational Site Charleston South Carolina
United States GSK Investigational Site Charlotte North Carolina
United States GSK Investigational Site Charlottesville Virginia
United States GSK Investigational Site Chattanooga Tennessee
United States GSK Investigational Site Chevy Chase Maryland
United States GSK Investigational Site Cincinnati Ohio
United States GSK Investigational Site Collegeville Pennsylvania
United States GSK Investigational Site Colorado Springs Colorado
United States GSK Investigational Site Coral Gables Florida
United States GSK Investigational Site Corsicana Texas
United States GSK Investigational Site Covington Louisiana
United States GSK Investigational Site Dallas Texas
United States GSK Investigational Site Dallas Texas
United States GSK Investigational Site Dallas Texas
United States GSK Investigational Site Denver Colorado
United States GSK Investigational Site Denver Colorado
United States GSK Investigational Site East Providence Rhode Island
United States GSK Investigational Site El Paso Texas
United States GSK Investigational Site El Paso Texas
United States GSK Investigational Site Eugene Oregon
United States GSK Investigational Site Fountain Valley California
United States GSK Investigational Site Germantown Tennessee
United States GSK Investigational Site Gibsonia Pennsylvania
United States GSK Investigational Site Greer South Carolina
United States GSK Investigational Site Houston Texas
United States GSK Investigational Site Houston Texas
United States GSK Investigational Site Huntington Beach California
United States GSK Investigational Site Iowa City Iowa
United States GSK Investigational Site Ithaca New York
United States GSK Investigational Site Kenilworth Illinois
United States GSK Investigational Site Killeen Texas
United States GSK Investigational Site Lafayette Louisiana
United States GSK Investigational Site Lake Oswego Oregon
United States GSK Investigational Site Lawrenceville Georgia
United States GSK Investigational Site Lilburn Georgia
United States GSK Investigational Site Little Rock Arkansas
United States GSK Investigational Site Long Beach California
United States GSK Investigational Site Los Angeles California
United States GSK Investigational Site Marietta Georgia
United States GSK Investigational Site Medford Oregon
United States GSK Investigational Site Metairie Louisiana
United States GSK Investigational Site Miami Florida
United States GSK Investigational Site Murray Utah
United States GSK Investigational Site North Andover Massachusetts
United States GSK Investigational Site North Olmsted Ohio
United States GSK Investigational Site Ocean New Jersey
United States GSK Investigational Site Oklahoma City Oklahoma
United States GSK Investigational Site Oklahoma City Oklahoma
United States GSK Investigational Site Omaha Nebraska
United States GSK Investigational Site Orange California
United States GSK Investigational Site Ozark Alabama
United States GSK Investigational Site Palmdale California
United States GSK Investigational Site Philadelphia Pennsylvania
United States GSK Investigational Site Philadelphia Pennsylvania
United States GSK Investigational Site Plano Texas
United States GSK Investigational Site Providence Rhode Island
United States GSK Investigational Site Riverside California
United States GSK Investigational Site Rolla Missouri
United States GSK Investigational Site San Antonio Texas
United States GSK Investigational Site San Antonio Texas
United States GSK Investigational Site San Diego California
United States GSK Investigational Site San Jose California
United States GSK Investigational Site Sarasota Florida
United States GSK Investigational Site Skillman New Jersey
United States GSK Investigational Site South Burlington Vermont
United States GSK Investigational Site Stockton California
United States GSK Investigational Site Sylvania Ohio
United States GSK Investigational Site Tampa Florida
United States GSK Investigational Site Tempe Arizona
United States GSK Investigational Site Vista California
United States GSK Investigational Site Waco Texas
United States GSK Investigational Site West Jordan Utah
United States GSK Investigational Site Wheat Ridge Colorado
United States GSK Investigational Site Winston-Salem North Carolina
United States GSK Investigational Site Ypsilanti Michigan

Sponsors (1)

Lead Sponsor Collaborator
GlaxoSmithKline

Country where clinical trial is conducted

United States, 

References & Publications (1)

This study has not been published in the scientific literature.

Outcome

Type Measure Description Time frame Safety issue
Primary Morning Peak Expiratory Flow
Secondary Total Nasal Symptom Scores Morning Forced Expiratory Volume in 1 Second Asthma Symptom-Free Days Asthma Rescue-Free Days
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