Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL

Completed · Not applicable

Conditions studied: Visual Acuity

In brief

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.

Key facts

Study ID

NCT00759096

Run by

Alcon Research

People needed

30

Starts

2007-05-01

Expected to finish

2008-07-01

Last updated by the study team

2023-12-05

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• ≥21 years of either gender or any race
• Potential post-op VA 20/20
• Pre-op astigmatism ≤ 1.0D
• Able to sign the informed consent
• Able to complete all required postoperative visits
• Planned cataract removal by phaco
• Clear intraocular media other than cataract

You may not qualify if…

• Signs of capsular tear, significant anterior chamber hyphema, or zonular rupture
• Any corneal pathology and previous corneal refractive surgery
• Patients with unrealistic expectations in anticipated post-op VA
• Happy to wear glasses
• Occupational night driver

Where it is running

• Alcon Call Center — Fort Worth, Texas, United States

Full record on ClinicalTrials.gov

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