Myopia Clinical Trial
Official title:
Evaluation of Outcomes Using the Amo Advanced CustomVue Ilasik Procedure
The purpose of this study is to assess the efficacy, predictability and safety of the Advanced CustomVue™ iLASIK procedure (WaveScan WaveFront® System, STAR S4 IR™ Excimer Laser System and IntraLase™ FS System).
Laser in situ keratomileusis (LASIK) surgery has been performed worldwide since 1990. More
recently, customized corneal ablation utilizing wavefront-sensing technology to determine the
optical aberration of a patient's cornea has optimized LASIK surgery results. Prior to the
introduction of wavefront-guided laser vision correction, the variables used for correcting
refractive errors were limited to sphere and cylinder. With the introduction of wavefront
laser vision correction surgeons are now able to provide individualized laser-induced corneal
tissue resection based not only on sphere and cylinder measurements, but also on an attempt
to treat 3rd through 6th higher-order aberrations (HOAs) utilizing Zernike polynomial
wavefront reconstructions and Fourier transformation.
Advanced Medical Optics, Inc. (AMO) has recently introduced the Advanced CustomVue™ iLASIK
procedure which utilizes the WaveScan WaveFront® System, a STAR S4 IR™ Excimer Laser System
and IntraLase™ FS System technology to provide the broadest range of wavefront-guided FDA
approved usages and an unprecedented level of precision and accuracy for patients undergoing
LASIK surgery. The procedure leverages Iris Registration, Fourier algorithms, VSS™ and VRR™
technologies and 3D ActiveTrak™ to ensure precise corneal ablation.1, 2
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