The objective of this study is to evaluate the Raindrop Near Vision Inlay for the
improvement of near vision in presbyopes implanted under a corneal flap or within a
Patients must require a reading add from +1.5 to +2.5 D, and both emmetropes as well as
ametropes (requiring concurrent LASIK) are included in the investigation. Suitable patients
will undergo implantation of the Raindrop inlay in the non-dominant eye to improve near
vision. If necessary, a LASIK excimer ablation will first be performed to optimize
postoperative vision at near and distance. Patients will follow a one-month regimen of strong
steroid, at a minimum, after corneal inlay implantation to facilitate healing and visual
Raindrop Near Vision Inlay
Clinical Study Identifier
Whitten Laser Eye
Last Modified on
8 November 2020
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
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