Fluticasone Nasal Spray Patient Preference Study
Completed · Phase 3
Conditions studied: Rhinitis, Allergic, Perennial
In brief
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.
Key facts
- Study ID
- NCT00398476
- Run by
- GlaxoSmithKline
- People needed
- 127
- Starts
- 2006-12-01
- Expected to finish
- 2006-12-04
- Last updated by the study team
- 2018-03-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- allergic rhinitis
- literate
You may not qualify if…
- clinical significant uncontrolled disease
- Use of intranasal corticosteroids (<4 weeks of FP [branded or generic],<4 week exposure to FF, <4 weeks use of other INS)
- Use of intranasal medications <1 week
- Use of meds that significantly inhibit CYP4503A4
- Use of perfume or oral rinse on study day
- Allergy/intolerance to INS, antihistamines, or excipients
- Positive pregnancy test or female who is breastfeeding
- Affiliation with investigational site
Where it is running
- GSK Investigational Site — Fountain Valley, California, United States
- GSK Investigational Site — Long Beach, California, United States
- GSK Investigational Site — San Diego, California, United States
- GSK Investigational Site — Denver, Colorado, United States
- GSK Investigational Site — Lakewood, Colorado, United States
- GSK Investigational Site — Lawrenceville, Georgia, United States
- GSK Investigational Site — Savannah, Georgia, United States
- GSK Investigational Site — Ypsilanti, Michigan, United States
- GSK Investigational Site — Minneapolis, Minnesota, United States
- GSK Investigational Site — Rolla, Missouri, United States
- GSK Investigational Site — St Louis, Missouri, United States
- GSK Investigational Site — Brick, New Jersey, United States
- GSK Investigational Site — Skillman, New Jersey, United States
- GSK Investigational Site — El Paso, Texas, United States
Full record on ClinicalTrials.gov
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