Trials / Completed
CompletedNCT01258309
Safety and Efficacy of Olopatadine Hydrochloride/Ketorolac Tromethamine Ophthalmic Solution Compared With Olopatadine Hydrochloride Ophthalmic Solution in Patients With Seasonal Allergic Conjunctivitis
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 129 (actual)
- Sponsor
- Allergan · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study will investigate the safety and efficacy of olopatadine hydrochloride / ketorolac tromethamine fixed dose combination ophthalmic solution compared with olopatadine hydrochloride ophthalmic solution in patients with seasonal allergic conjunctivitis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | olopatadine hydrochloride /ketorolac tromethamine fixed dose combination ophthalmic solution | One drop of olopatadine hydrochloride/ketorolac tromethamine fixed dose combination ophthalmic solution administered to each eye, twice daily for 21 days. |
| DRUG | olopatadine hydrochloride 0.1% ophthalmic solution | One drop of olopatadine hydrochloride 0.1% ophthalmic solution administered to each eye, twice daily for 21 days. |
Timeline
- Start date
- 2010-12-01
- Primary completion
- 2011-01-01
- Completion
- 2011-01-01
- First posted
- 2010-12-10
- Last updated
- 2012-01-25
Locations
1 site across 1 country: India
Source: ClinicalTrials.gov record NCT01258309. Inclusion in this directory is not an endorsement.