Last updated on May 2020

Wavefront-guided LASIK for Monovision Treatment of Myopic Subjects With Presbyopia


Brief description of study

This study will be a 12-month, prospective, multicenter, open-label, non-comparative, non-randomized clinical investigation conducted at 10 to 14 sites. A total of 383 subjects will be enrolled to achieve approximately 268 treated subjects, resulting in at least 241 evaluable subjects at the point of refractive stability. After signing the informed consent, subjects meeting all inclusion and exclusion criteria in both eyes may be scheduled for surgery. The follow-up visit schedule will be the same for each operative eye.

Clinical Study Identifier: NCT04075591

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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