A Study to Compare a New Eye Drop Formulation With Systane® Gel Drops and Genteal® Lubricant Gel Drops for Moderate to Severe Dry Eye Relief
Completed · Phase 3
Conditions studied: Dry Eye Syndromes
In brief
A study to evaluate the tolerability and acceptability of an investigational eye drop formulation in patients with Dry Eye Disease.
Key facts
- Study ID
- NCT02455050
- Run by
- Allergan
- People needed
- 79
- Starts
- 2014-12-01
- Expected to finish
- 2015-08-01
- Last updated by the study team
- 2017-01-04
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Current use of an artificial tear product
- Visual Acuity of at least 20/40 (while wearing glasses, if necessary).
You may not qualify if…
- Use of contact lenses in the last 3 months, or anticipated use of contact lenses during the study
- Cataract surgery, laser-assisted in situ keratomileusis (LASIK), photorefractive keratectomy within 6 months
- Use of RESTASIS® Cyclosporine Ophthalmic Emulsion or any topical cyclosporine within 3 months
- Diagnosis of glaucoma.
Where it is running
- Study site — Azusa, California, United States
Full record on ClinicalTrials.gov
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