Surgeon Experience ReSTOR A +4 Intraocular Lens (IOL)

Completed

Conditions studied: Cataract

In brief

To collect visual outcome data post AcrySof ReSTOR Aspheric +4 implantation from surgeons throughout the United States.

Key facts

Study ID

NCT00733512

Run by

Alcon Research

People needed

146

Starts

2007-06-01

Expected to finish

2008-03-01

Last updated by the study team

2017-03-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• operable cataracts; candidate for presbyopic correcting intraocular lens (IOL)

You may not qualify if…

• ocular comorbidities confounding study outcomes

Where it is running

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

Full record on ClinicalTrials.gov

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