Evaluation of Outcomes Using the AMO Advanced Customvue™ iLasik Procedure

Vision Correction Clinical Trial

Official title:
Evaluation of Outcomes Using the AMO Advanced Customvue™ iLasik Procedure (Wavescan Wavefront® System, Star S4 IR™ Excimer Laser System and Intralse™ FS System)

Status Completed

Clinical Trial Summary

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). Patient data will be collected electronically and analyzed to determine improvements in postoperative visual acuity, visual quality and residual error.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Vision Correction

Clinical Trial Details

NCT number	NCT01061294
Study type	Interventional
Source	Innovative Medical
Contact
Status	Completed
Phase	Phase 4
Start date	December 2009
Completion date	December 2010

View Details

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