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

Completed · Not applicable

Conditions studied: Dry Eye Syndrome

In brief

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

Key facts

Study ID

NCT00544713

Run by

Allergan

People needed

228

Starts

2007-09-01

Expected to finish

2008-06-01

Last updated by the study team

2011-12-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

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

You may not qualify if…

• 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

Where it is running

• Study site — San Diego, California, United States

Full record on ClinicalTrials.gov

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