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Clinical Trial Summary

The purpose of this study is to demonstrate effective symptom relief with the use of Systane Complete among subjects with dry eye disease (DED).


Clinical Trial Description

Subjects will be expected to attend a screening/baseline visit and one additional visit at Day 28 (± 2 days), with a telephone call visit conducted at Day 14 (± 2 days). Individual duration of subject participation will be approximately 28 days. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05056155
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date November 9, 2021
Completion date March 25, 2022

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