Expired Study
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Fort Worth, Texas 76134


The purpose of this study is to evaluate the thickness accuracy of Laser-assisted in situ keratomileusis (LASIK) flaps created with the LenSx® Laser.


Inclusion Criteria: - Diagnosed with myopia or hyperopia and eligible for femtosecond laser initiated LASIK surgery; - Best corrected visual acuity (BCVA) correctable to at least 20/25 in each eye; - If contact lens wearer, willing to discontinue contact lens wear prior to screening procedures; - Willing and able to return for ALL scheduled follow-up examinations; - Willing and able to provide written informed consent; - Eligible for bilateral LASIK procedures to be done on the same day; - Other protocol-specified inclusion criteria may apply. Exclusion Criteria: - Previous corneal surgery, corneal lesions that will impede laser treatment, corneal edema, hypotony, glaucoma, existing corneal implant, or keratoconus; - Known sensitivity to planned study concomitant medications; - Participation in any other ophthalmic drug or device clinical study for 30 days prior to or during the time of participation in this study; - Irregular astigmatism, based on the Investigator's judgement; - Pregnant, lactating or planning to become pregnant during the course of the study; - Other protocol-specified exclusion criteria may apply.



Primary Contact:

Study Director
Clinical Trial Manager, GCRA
Alcon, A Novartis Division

Backup Contact:


Location Contact:

Fort Worth, Texas 76134
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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