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Efficacy Study of Ketorolac and HPMC to Treat Dry Eye

Dry Eye Clinical Trial

Official title:
A Double-Masked, Randomized, Single-Center Study Evaluating the Effect of 0.30% Ketorolac/0.80% HPMC, 0.80% HPMC and Vehicle on Symptoms of Dry Eye After Exposure to the Controlled Adverse Environment (CAE)

Clinical Trial Summary

The purpose of this study is to determine whether ketorolac and Hydroxypropyl Methylcellulose are effective in the treatment of Dry Eye.

Clinical Trial Description

This is a double masked, randomized study with approximately 45 subjects randomized to one of the three treatment arms at a single site. There are 5 visits over the course of 16 days. Visit 1: Day -7 Visit 2: Day 0 Visit 3: Day 2 Visit 4: Day 7 Visit 5: Day 9 ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03693183
Study type Interventional
Source ORA, Inc.
Contact
Status Withdrawn
Phase Phase 2
Start date March 2009
Completion date June 15, 2009
View Details
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