Clinical Outcomes Following Treatment With SYSTANE® BALANCE



Status:Completed
Conditions:Ocular
Therapuetic Areas:Ophthalmology
Healthy:No
Age Range:18 - Any
Updated:5/12/2018
Start Date:July 29, 2016
End Date:November 2017

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Clinical Evaluation Following Use of SYSTANE® BALANCE in Subjects With Lipid-Deficient Dry Eye

The purpose of this study is to evaluate the clinical effectiveness of SYSTANE® BALANCE
compared to REFRESH OPTIVE® Advanced in subjects with lipid-deficient dry eye.


Inclusion Criteria:

- Willing and able to attend all study visits;

- Must sign an informed consent form;

- Best-corrected visual acuity (BCVA) of 55 letters or better in each eye as assessed
using an early treatment diabetic retinopathy study (ETDRS) chart;

- Willing to take study products as directed for entire study;

- Other protocol-specified inclusion criteria may apply.

Exclusion Criteria:

- Women of childbearing potential who are pregnant, plan to become pregnant during the
study, breast feeding, or not using adequate birth control methods;

- Contact lens use within 30 days prior to Screening Visit, or unwilling to avoid
contact lens use during the course of the study;

- Use of medication excluded by the protocol;

- Diseases, illnesses, infections, or ocular abnormalities excluded by the protocol;

- Ocular surgeries or procedures excluded by the protocol;

- Other protocol-specified exclusion criteria may apply.
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