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Completed Phase 4 Interventional Results available

Comparator Study Evaluating Patient Experience And Preference Of FFNS vs. FPNS

ClinicalTrials.gov ID: NCT00519636

Public ClinicalTrials.gov record NCT00519636. 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 Jul 22, 2026, 8:31 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 Randomized, Double-blind, Placebo-controlled, Active Comparator, One-Week, Cross-Over, Multicenter Study to Evaluate the Efficacy and Patient Preference of Nasal Spray Characteristics of Once-Daily, Intranasal Administration of 110mcg Fluticasone Furoate Nasal Spray and 200mcg Fluticasone Propionate Nasal Spray in Adult Subjects With Seasonal Allergic Rhinitis

Study identification

NCT ID
NCT00519636
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
360 participants

Conditions and interventions

Interventions

  • FPNS Drug
  • FFNS Drug
  • placebo FFNS Drug
  • placebo FPNS Drug

Drug

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
Jul 31, 2007
Primary completion
Oct 31, 2007
Completion
Oct 31, 2007
Last update posted
Dec 8, 2016

2007

United States locations

U.S. sites
28
U.S. states
12
U.S. cities
23
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35209
GSK Investigational Site Phoenix Arizona 85050
GSK Investigational Site Long Beach California 90806
GSK Investigational Site Los Angeles California 90025
GSK Investigational Site San Diego California 92120
GSK Investigational Site San Diego California 92123
GSK Investigational Site San Francisco California 94104
GSK Investigational Site San Jose California 95117
GSK Investigational Site Vista California 92083
GSK Investigational Site Tallahassee Florida 32308
GSK Investigational Site Lilburn Georgia 30047
GSK Investigational Site Bangor Maine 04401
GSK Investigational Site Bethesda Maryland 20814
GSK Investigational Site Ocean City New Jersey 07712
GSK Investigational Site Ithaca New York 14850
GSK Investigational Site Rockville Centre New York 11570
GSK Investigational Site Collegeville Pennsylvania 19426
GSK Investigational Site Philadelphia Pennsylvania 19107
GSK Investigational Site Philadelphia Pennsylvania 19115
GSK Investigational Site Charleston South Carolina 29406
GSK Investigational Site Austin Texas 78731
GSK Investigational Site Austin Texas 78750
GSK Investigational Site Dallas Texas 75230
GSK Investigational Site Dallas Texas 75231
GSK Investigational Site Dallas Texas 75246
GSK Investigational Site El Paso Texas 79925
GSK Investigational Site New Braunfels Texas 78130
GSK Investigational Site San Antonio Texas 78229

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 NCT00519636, 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 8, 2016 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00519636 live on ClinicalTrials.gov.

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