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 |
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.
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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