Clinical Trials Directory

Trials / Completed

CompletedNCT00789555

Safety of PATANASE Nasal Spray in Patients With Perennial Allergic Rhinitis

Safety of PATANASE® Nasal Spray in Patients With Perennial Allergic Rhinitis

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
1,260 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
12 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to assess local nasal adverse effects, as well as systemic effects, of PATANASE nasal spray when compared with Patanase Vehicle, pH 3.7 and Patanase Vehicle, pH 7.0 in patients with perennial allergic rhinitis (PAR).

Conditions

Interventions

TypeNameDescription
DRUGOlopatadine hydrochloride 0.6% nasal spray (PATANASE)Two sprays in each nostril twice a day (morning and evening) for up to 12 months
OTHEROlopatadine nasal spray vehicle, pH 3.7Two sprays in each nostril twice a day (morning and evening) for up to 12 months
OTHEROlopatadine nasal spray vehicle, pH 7.0Two sprays in each nostril twice a day (morning and evening) for up to 12 months

Timeline

Start date
2008-11-01
Primary completion
2011-01-01
Completion
2011-01-01
First posted
2008-11-13
Last updated
2018-02-08
Results posted
2012-09-07

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00789555. Inclusion in this directory is not an endorsement.