Clinical Trials Directory

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

TypeNameDescription
DRUGolopatadine hydrochloride /ketorolac tromethamine fixed dose combination ophthalmic solutionOne drop of olopatadine hydrochloride/ketorolac tromethamine fixed dose combination ophthalmic solution administered to each eye, twice daily for 21 days.
DRUGolopatadine hydrochloride 0.1% ophthalmic solutionOne 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.