Clinical Evaluation of Systane Ultra Compared to Optive in Ocular Surface Staining
Status: | Completed |
---|---|
Conditions: | Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 5/5/2014 |
Start Date: | July 2013 |
End Date: | June 2014 |
Contact: | Alcon Call Center |
Email: | alcon.medinfo@alcon.com |
Phone: | 1-888-451-3937 |
The purpose of this study is to compare Systane Ultra lubricant eye drops to Optive
lubricating eye drops for ocular surface staining within dry eye subjects and to evaluate
the safety of Systane Ultra after 3 months of use.
lubricating eye drops for ocular surface staining within dry eye subjects and to evaluate
the safety of Systane Ultra after 3 months of use.
Following a 2-week washout phase with saline eye drops, subjects will be randomized to
receive either Systane Ultra or Optive for the remainder of the study.
receive either Systane Ultra or Optive for the remainder of the study.
Inclusion Criteria:
- Willing and able to attend all study visits.
- Diagnosis of dry eye, as specified in protocol.
- Uses artificial tears, as specified in protocol.
- Other protocol-defined inclusion criteria may apply.
Exclusion Criteria:
- Poor visual acuity, as specified in protocol.
- Women of childbearing potential who are pregnant, lactating, or not using adequate
birth control, as specified in protocol.
- Any hypersensitivity or allergy to the investigational products or ingredients.
- Any eye disorder, ocular surgery, medication, medical condition, or systemic disease,
as specified in protocol.
- Contact lens use within 2 weeks of Screening Visit.
- Other protocol-defined exclusion criteria may apply.
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