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Completed Phase 3 Interventional Results available

Fluticasone Nasal Spray Patient Preference Study

ClinicalTrials.gov ID: NCT00398476

Public ClinicalTrials.gov record NCT00398476. 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, 8:21 AM EST

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Official title

A Patient Preference Evaluation Study of Fluticasone Furoate Nasal Spray and Fluticasone Propionate Aqueous Nasal Spray in Subject With Allergic Rhinitis

Brief summary

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

The objectives of this study are to evaluate and compare patient preference for FF (Fluticasone Furoate) and FP (Fluticasone Propionate Aqueous)nasal sprays in the treatment of allergic rhinitis following single-dose administration.

Study identification

NCT ID
NCT00398476
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
127 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Dec 1, 2006 (Actual)
Primary completion
Dec 4, 2006 (Actual)
Completion
Dec 4, 2006 (Actual)
Last update posted
Mar 1, 2018

2006

United States locations

U.S. sites
14
U.S. states
8
U.S. cities
14
Facility City State ZIP Site status
GSK Investigational Site Fountain Valley California 92708 —
GSK Investigational Site Long Beach California 90808 —
GSK Investigational Site San Diego California 92123 —
GSK Investigational Site Denver Colorado 80230 —
GSK Investigational Site Lakewood Colorado 80401 —
GSK Investigational Site Lawrenceville Georgia 30045 —
GSK Investigational Site Savannah Georgia 31406 —
GSK Investigational Site Ypsilanti Michigan 48197 —
GSK Investigational Site Minneapolis Minnesota 55402 —
GSK Investigational Site Rolla Missouri 65401 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Brick New Jersey 8724 —
GSK Investigational Site Skillman New Jersey 08558 —
GSK Investigational Site El Paso Texas 79925 —

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 NCT00398476, 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 Mar 1, 2018 · 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 NCT00398476 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →