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Completed Phase 3 Interventional Results available

Once-Daily Investigational Nasal Spray In Adults And Adolescents With Vasomotor Rhinitis

ClinicalTrials.gov ID: NCT00118703

Public ClinicalTrials.gov record NCT00118703. 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 Nov 10, 2026, 5:35 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 4 Week Randomized, Double Blind, Placebo Controlled Study of GW685698X Aq Nasal Spray 100mcg QD in Adults and Adolescents With Vasomotor Rhinitis

Brief summary

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

The primary objective of this study is to compare the efficacy and safety of GW685698X 100mcg once daily (QD) aqueous nasal spray with vehicle placebo nasal spray in adult and adolescent subjects (12 years of age and older) with vasomotor rhinitis (VMR).

Study identification

NCT ID
NCT00118703
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
350 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
Jul 1, 2005 (Type not available)
Primary completion
Feb 1, 2006 (Actual)
Completion
Feb 9, 2006 (Actual)
Last update posted
Aug 21, 2017

2005 – 2006

United States locations

U.S. sites
40
U.S. states
23
U.S. cities
38
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35209 —
GSK Investigational Site Phoenix Arizona 85012 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Fresno California 93720 —
GSK Investigational Site Irvine California 92618 —
GSK Investigational Site Los Angeles California 90025 —
GSK Investigational Site Orange California 92868 —
GSK Investigational Site Paramount California 90723 —
GSK Investigational Site Sacramento California 95819 —
GSK Investigational Site San Francisco California 94102 —
GSK Investigational Site San Jose California 95128 —
GSK Investigational Site Walnut Creek California 94598 —
GSK Investigational Site Englewood Colorado 80112 —
GSK Investigational Site Miami Florida 33173 —
GSK Investigational Site Sarasota Florida 34233 —
GSK Investigational Site Tallahassee Florida 32308 —
GSK Investigational Site Vero Beach Florida 32960 —
GSK Investigational Site Stockbridge Georgia 30281 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Chicago Illinois 60632 —
GSK Investigational Site South Bend Indiana 46617 —
GSK Investigational Site Shreveport Louisiana 71105 —
GSK Investigational Site Bethesda Maryland 20814 —
GSK Investigational Site Wheaton Maryland 20902 —
GSK Investigational Site North Dartmouth Massachusetts 02747 —
GSK Investigational Site Detroit Michigan 48202 —
GSK Investigational Site Jackson Mississippi 39202 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Brick New Jersey 8724 —
GSK Investigational Site Skillman New Jersey 08558 —
GSK Investigational Site Ithaca New York 14850 —
GSK Investigational Site Rochester New York 14618 —
GSK Investigational Site Sylvania Ohio 43560 —
GSK Investigational Site Blue Bell Pennsylvania 19422 —
GSK Investigational Site Providence Rhode Island 2906 —
GSK Investigational Site Chattanooga Tennessee 37421 —
GSK Investigational Site Dallas Texas 75231-4307 —
GSK Investigational Site Dallas Texas 75231 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site South Burlington Vermont 05403 —

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 19 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00118703, 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 21, 2017 · Synced Nov 10, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00118703 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →