Expired Study
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San Diego, California


Purpose:

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


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


NCT ID:

NCT00544713


Primary Contact:

Study Director
Medical Director
Allergan


Backup Contact:

N/A


Location Contact:

San Diego, California
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 21, 2017

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