Evaluation of Blink Tears and Systane Concomitant With Restasis for the Treatment of Dry Eye Symptoms
Completed · Not applicable
Conditions studied: Dry Eye Syndrome
In brief
The purpose of this study is to evaluate the efficacy of Blink Tears and Systane used concomitantly with topical cyclosporine for the treatment of dry eye.
Key facts
- Study ID
- NCT00565669
- Run by
- Medical University of South Carolina
- People needed
- 20
- Starts
- 2007-10-01
- Expected to finish
- 2008-10-01
- Last updated by the study team
- 2018-11-07
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subject must have dry eye.
- Age: 18 years and older.
- Males or females
- Up to grade 3 conjunctival staining.
- Score of no more than 4 on the Subjective Evaluation of Symptoms of Dryness (SESOD) at screening.
- Currently using Restasis to treat dry eye syndrome (at least for 3 months prior to enrollment).
- Willing and able to comply with scheduled visits and other study procedures.
You may not qualify if…
- Prior unsuccessful use of topical cyclosporine (defined as patients taking it at least 3 months without improvement.
- Known contraindications to any study medication or ingredients.
- Planned use of contact lenses (unless discontinued use more than 30 days prior to randomization.
- Contact lens use during the active treatment portion of the trial.
- Active ocular allergies.
- Ocular surgery within the past 3 months.
- Any concurrent infectious/non infectious conjunctivitis, keratitis or uveitis.
- Active ocular diseases or uncontrolled systemic disease (blepharitis patients that are actively being treated or disease that is uncontrollable.
- Pregnant or nursing mothers and females of childbearing potential not practicing a reliable and medically acceptable method of birth control.
- Participation in (or current participation) any investigational drug or device trial.
- Conjuctival staining grade 4.
Where it is running
- Medical University of South Carolina, Storm Eye Institute — Charleston, South Carolina, United States
Full record on ClinicalTrials.gov
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