Visual Performance of Bilateral AcrySof ReSTOR Aspheric +4

Completed

Conditions studied: Cataract

In brief

Determine the clinical visual outcomes following bilateral implantation of the AcrySof ReSTOR Aspheric Intraocular Lens (IOL) and to demonstrate what percentage of the subjects obtain spectacle freedom.

Key facts

Study ID

NCT01215045

Run by

Alcon Research

People needed

17

Starts

2007-06-01

Expected to finish

2008-05-01

Last updated by the study team

2010-10-05

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…

• Preexisting conditions confounding results; > 1 Diopter preoperative astigmatism

Where it is running

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

Full record on ClinicalTrials.gov

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