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Residence Time Evaluation of Systane Ultra Lubricant Eye Drops vs. Hialid and Saline

Dry Eye Syndrome Clinical Trial

Clinical Trial Summary

The purpose of this study is to evaluate the ocular retention time of Systane Ultra compared to Hialid and saline.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01252121
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date October 2010
Completion date June 2011
View Details
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