Status:
COMPLETED
Single Dose Crossover Study of Patient Preference for Unscented Nasonex® Nasal Spray Versus Scented Flonase® Nasal Spray (Study P04207)
Lead Sponsor:
Organon and Co
Conditions:
Allergic Rhinitis
Eligibility:
All Genders
18-65 years
Phase:
PHASE4
Brief Summary
This was a one-day single dose trial conducted to compare patient's preference for Nasonex® (mometasone) versus Flonase® nasal spray. Each patient was randomized to take one dose (2 sprays in each nos...
Eligibility Criteria
Inclusion
- Subject must have been 18-65 years of age, of either sex and any race.
- Subject must have had symptomatic allergic rhinitis with a total nasal symptom (congestion, rhinorrhea, sneezing, itching) severity score of \<6 but \>2; congestion must have been \<2.
- Subject must have been free of any clinically significant disease (other than allergic rhinitis) that would interfere with study evaluations.
- Subject must have understood and been able to adhere to the dosing and visit schedule.
Exclusion
- Subject had used any investigational product within 30 days prior to enrollment.
- Subject was in a situation or condition that, in the opinion of the investigator, may have interfered with optimal participation in the study.
- Subject was participating in any other clinical study(ies).
- Subject was using any nasal lavage fluid or spray.
- Subject was using any perfume during the study day.
- Subject was using any oral rinse during the study day.
- Subject had used topical or oral nasal decongestants in the past 1 week.
- Subject had used a nasal corticosteroid in the previous 2 weeks.
- Subject had anosmia or ageusia (absence of the sense of smell or taste).
- Subject had been using medications which are associated with anosmia or ageusia in the 2 weeks prior to testing.
- Subject had a respiratory infection in the 2 weeks prior to testing.
Key Trial Info
Start Date :
December 1 2004
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2005
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT00817050
Start Date
December 1 2004
End Date
January 1 2005
Last Update
August 15 2024
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