Visual Function Evaluation of Bilateral AcrySof ReSTOR Aspheric IOL

Completed · Phase 4

Conditions studied: Cataracts

In brief

The objective of this study is to evaluate postoperative visual function in patients implanted bilaterally with the ReSTOR Aspheric Intraocular Lens (IOL).

Key facts

Study ID

NCT00818116

Run by

Alcon Research

People needed

34

Starts

2008-12-01

Last updated by the study team

2010-07-30

Who can join

Age: 50 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Bilateral cataract patients who require natural crystalline lens removal and bilateral Intraocular Lens (IOL) implantation.
• 50\~75 years of age
• <1 Diopter of astigmatism preoperatively (before surgery) as measured by Keratometry readings.

You may not qualify if…

• Patients with pre-existing conditions that could skew the results.
• Any of conditions before and during surgery specified in the product information.

Where it is running

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

Full record on ClinicalTrials.gov

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