Clinical Trials Directory

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

TypeNameDescription
DRUGCyclosporine, Refresh PlusCyclosporine 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.