Trials / Completed
CompletedNCT00349440
Efficacy of Cyclosporine for the Prevention and Treatment of Dry Eye Symptoms Following LASIK or Photorefractive Keratectomy
Efficacy of Topical Cyclosporine Ophthalmic Emulsion for the Prevention and Treatment of Dry Eye Symptoms Following LASIK or Photorefractive Keratectomy
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 93 (actual)
- Sponsor
- Innovative Medical · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the effect of topical cyclosporine ophthalmic solution 0.05% (Restasis, Allergan) on the signs and symptoms of dry eye in patients undergoing LASIK or photorefractive keratectomy (PRK).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Cyclosporine, Refresh Plus | Cyclosporine 0.4ml (in the eye) on for 3 months instill one drop in randomized eye twice daily. Refresh Plus 0.4ml (in the eye) on for 3 months instill one drop in randomized eye twice daily. |
Timeline
- Start date
- 2006-09-01
- Primary completion
- 2008-09-01
- Completion
- 2008-09-01
- First posted
- 2006-07-07
- Last updated
- 2008-09-26
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00349440. Inclusion in this directory is not an endorsement.