Evaluate the Safety and Efficacy of a New Artificial Tear for Use After LASIK Surgery

• Status: Completed
• Trial end date: 2008-06-01
• Target enrollment: 0
• Participant gender: All

Summary

This study will evaluate the safety and efficacy of a new artificial tear for the treatment of dry eye that may occur after LASIK surgery

• Phase: N/A
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Allergan
• Treatments: Carboxymethylcellulose Sodium; Glycerol; Lubricant Eye Drops

Criteria

Inclusion Criteria:

• Candidate for bilateral LASIK surgery for myopia correction in the range of -1.00 to -8.00 diopters

Exclusion Criteria:

• Dry eye signs and symptoms

• Preoperative soft or rigid contact lens wear within last 7 or 30 days, respectively

• Pregnancy or planning pregnancy

• Uncontrolled systemic disease

• Use of systemic medications affecting dry eye