Clinical Trials Directory

Trials / Completed

CompletedNCT00405431

Will Restasis Eye Drops Increase Your Chance of Having a Successful Surgery?

Influence of Post-Operative Cyclosporine 0.05% (Restasis) on the Success of Glaucoma Filtering Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
43 (actual)
Sponsor
Wills Eye · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether reducing inflammation of the surface of the eye with topical Restasis after glaucoma surgery will improve surgical outcomes and increase patient comfort.

Detailed description

Continued use of glaucoma drops can alter the outer surface of the eye and result in swelling and irritation, changing the structure of the eye. This structural change has been found to be a significant risk factor for the failure of glaucoma surgery. A comparison of how well patients do after glaucoma surgery depending on whether they use Restasis (the only prescription medication approved by the FDA for treating dry eye) or artificial tears (which can be purchased without a prescription) for 6 months following their surgery.

Conditions

Interventions

TypeNameDescription
DRUGRestasis1 drop in study eye twice a day X 6 months
DRUGEndura (artificial tears)1 drop in study eye twice a day X 6 months

Timeline

Start date
2004-03-01
Primary completion
2005-06-01
Completion
2007-11-01
First posted
2006-11-30
Last updated
2016-11-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00405431. Inclusion in this directory is not an endorsement.