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| Sponsor: | GlaxoSmithKline |
|---|---|
| Information provided by: | GlaxoSmithKline |
| ClinicalTrials.gov Identifier: | NCT00398476 |
Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Rhinitis, Allergic, Perennial Allergic Rhinitis (Disorder) |
Drug: fluticasone propionate Drug: fluticasone furoate |
Phase III |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Crossover Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | A Patient Preference Evaluation Study of Fluticasone Furoate Nasal Spray and Fluticasone Propionate Aqueous Nasal Spray in Subject With Allergic Rhinitis |
| Estimated Enrollment: | 125 |
| Study Start Date: | December 2006 |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, California | |
| GSK Investigational Site | |
| Fountain Valley, California, United States, 92708 | |
| GSK Investigational Site | |
| Long Beach, California, United States, 90808 | |
| GSK Investigational Site | |
| San Diego, California, United States, 92123 | |
| United States, Colorado | |
| GSK Investigational Site | |
| Denver, Colorado, United States, 80230 | |
| GSK Investigational Site | |
| Lakewood, Colorado, United States, 80401 | |
| United States, Georgia | |
| GSK Investigational Site | |
| Lawrenceville, Georgia, United States, 30045 | |
| GSK Investigational Site | |
| Savannah, Georgia, United States, 31406 | |
| United States, Michigan | |
| GSK Investigational Site | |
| Ypsilanti, Michigan, United States, 48197 | |
| United States, Minnesota | |
| GSK Investigational Site | |
| Minneapolis, Minnesota, United States, 55402 | |
| United States, Missouri | |
| GSK Investigational Site | |
| Rolla, Missouri, United States, 65401 | |
| GSK Investigational Site | |
| St. Louis, Missouri, United States, 63141 | |
| United States, New Jersey | |
| GSK Investigational Site | |
| Brick, New Jersey, United States, 8724 | |
| GSK Investigational Site | |
| Skillman, New Jersey, United States, 08558 | |
| United States, Texas | |
| GSK Investigational Site | |
| El Paso, Texas, United States, 79925 | |
| Study Director: | GSK Clinical Trials | GlaxoSmithKline |
More Information
| Responsible Party: | Cheri Hudson; Clinical Disclosure Advisor, GSK Clinical Disclosure |
| ClinicalTrials.gov Identifier: | NCT00398476 History of Changes |
| Other Study ID Numbers: | FFU108556 |
| Study First Received: | November 9, 2006 |
| Last Updated: | March 17, 2011 |
| Health Authority: | United States: Food and Drug Administration |
|
taste questionnaire preference attributes |
odor after taste scent |
|
Rhinitis Rhinitis, Allergic, Perennial Nose Diseases Respiratory Tract Diseases Respiratory Tract Infections Otorhinolaryngologic Diseases Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases Fluticasone |
Bronchodilator Agents Autonomic Agents Peripheral Nervous System Agents Physiological Effects of Drugs Pharmacologic Actions Anti-Asthmatic Agents Respiratory System Agents Therapeutic Uses Dermatologic Agents Anti-Allergic Agents Anti-Inflammatory Agents |