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
| Type | Name | Description |
|---|---|---|
| DRUG | Olopatadine hydrochloride 0.6% nasal spray (PATANASE) | Two sprays in each nostril twice a day (morning and evening) for up to 12 months |
| OTHER | Olopatadine nasal spray vehicle, pH 3.7 | Two sprays in each nostril twice a day (morning and evening) for up to 12 months |
| OTHER | Olopatadine nasal spray vehicle, pH 7.0 | Two 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.