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
| Type | Name | Description |
|---|---|---|
| DRUG | Restasis | 1 drop in study eye twice a day X 6 months |
| DRUG | Endura (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.