Fluticasone Nasal Spray Patient Preference Study
| Status: | Completed |
|---|---|
| Conditions: | Allergy |
| Therapuetic Areas: | Otolaryngology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/17/2018 |
| Start Date: | December 1, 2006 |
| End Date: | December 4, 2006 |
A Patient Preference Evaluation Study of Fluticasone Furoate Nasal Spray and Fluticasone Propionate Aqueous Nasal Spray in Subject With Allergic Rhinitis
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.
(Fluticasone Furoate) and FP (Fluticasone Propionate Aqueous)nasal sprays in the treatment of
allergic rhinitis following single-dose administration.
Inclusion Criteria:
- allergic rhinitis
- literate
Exclusion Criteria:
- 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
We found this trial at
14
sites
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