Evaluation of Maintaining Visual Performance in Participants Who Engage in Electronic Visual Tasking While Using Restasis®
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Ocular |
| Therapuetic Areas: | Ophthalmology |
| Healthy: | No |
| Age Range: | 18 - 55 |
| Updated: | 4/21/2016 |
| Start Date: | July 2015 |
| End Date: | July 2016 |
This study will evaluate the efficacy of Restasis® in participants with dry eye disease who
engage in electronic visual tasking.
engage in electronic visual tasking.
Inclusion:
- Has Eye Symptoms when using video display terminals
- Has a reported history of dry eye in both eyes.
Exclusion:
- Diagnosed with eye infection or active inflammation.
- Has worn contact lenses within the past 7 days or anticipated use during the study.
- Has used any eye drops within 2 hours.
- Has had laser-assisted in situ keratomileusis (LASIK) within 12 months.
- Has used Restasis® within 90 days.
- Has had any eye and or/lid surgeries within 6 months.
- Has had cataract surgery in either eye.
- Has current punctal occlusion or anticipate a change in punctal occlusion status at
any point during the study.
- Is currently taking any topical ophthalmic prescriptions or over-the-counter
solutions, artificial tears, gels or lid scrubs that cannot be discontinued for the
trial duration.
- Use of medication known to cause ocular drying that is not on a stable dose for at
least 30 days.
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