Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal

Clinical Trial Summary

The purpose of this study is to assess uniocular and binocular unaided distance, intermediate, and near VA; contrast sensitivity, accommodation amplitude, stereopsis, glare testing, ocular aberrations and the clinical satisfaction assessment after bilateral implant of the Restor IOL.

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NCT number	NCT00759096
Study type	Interventional
Source	Alcon Research
Contact
Status	Completed
Phase	N/A
Start date	May 2007
Completion date	July 2008

Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms