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Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness of the modified Conjunctival Allergen Challenge (CAC) and observe how the produced allergic inflammation reacts to treatment with a proven ocular anti-inflammatory medication,

Prednisolone, assessed by the following measures:

- Ocular itching

- Conjunctival redness


Clinical Trial Description

Prospective, single center, randomized, double-masked, placebo controlled study. Subjects will be randomized to one of the following treatment arms to dose four times per day (QID) for 8 days between Visits 4 and 5.

- Prednisolone phosphate

- Tears Naturale II Ophthalmic Solution (Placebo)

Duration:

Approximately 19 days

Controls:

Artificial Tears (Tears Naturale® II) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01534195
Study type Interventional
Source ORA, Inc.
Contact
Status Completed
Phase Phase 4
Start date January 2012
Completion date February 2012

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