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Clinical Trial Summary

The purpose of this study is to characterize the safety and effectiveness of the ACRYSOF IQ ReSTOR +2.5 diopter (D) Multifocal Toric Intraocular Lens (IOL) in subjects at least 3 months and no more than 14 months after IOL implantation.


Clinical Trial Description

This is a retrospective and prospective clinical study comprised of a retrospective chart review for preoperative, surgical and early postoperative data, and a prospective postoperative visit conducted at least 3 months but not more than 14 months after IOL implantation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02176343
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date July 21, 2014
Completion date August 22, 2014

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