Visual Function After Implantation of Bilateral AcrySof ReSTOR Aspheric +3

Completed · Phase 4

Conditions studied: Cataract

In brief

A prospective evaluation of the visual parameters in a series of patients bilaterally implanted with AcrySof ReSTOR +3 Intraocular Lens (IOL).

Key facts

Study ID

NCT00719732

Run by

Alcon Research

People needed

218

Starts

2007-09-01

Expected to finish

2009-05-01

Last updated by the study team

2010-03-16

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Diagnosed with cataracts

You may not qualify if…

• Pre-existing conditions that could skew the results or are contraindications for the ReSTOR intraocular lens;
• <1 diopter astigmatism by keratometry readings.

Where it is running

• Alcon Call Center for Trial Locations — Fort Worth, Texas, United States

Full record on ClinicalTrials.gov

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