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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of Systane® Balance following 90 days of QID (4 times/day) dosing among Indian subjects with dry eye.


Clinical Trial Description

This study was conducted in India. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02511379
Study type Interventional
Source Alcon Research
Contact
Status Terminated
Phase N/A
Start date November 26, 2015
Completion date June 20, 2016

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