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Clinical Trial Summary

The purpose of this clinical research study is to investigate the efficacy of predosing patients undergoing cataract surgery with the potent corticosteroid difluprednate ophthalmic emulsion 0.05% compared to prednisolone acetate 1% on corneal edema (swelling), and retinal thickness.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01244334
Study type Interventional
Source Cincinnati Eye Institute Northern Kentucky
Contact
Status Completed
Phase Phase 4
Start date March 2009
Completion date November 2010

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