Presbyopia-Correcting Intraocular Lenses (IOLs)

Completed · Phase 4

Conditions studied: Cataract

In brief

The purpose of this study is to prospectively evaluate postoperative visual and refractive parameters in a series of subjects bilaterally implanted with Presbyopia-Correcting Intraocular Lenses (IOLs).

Key facts

Study ID

NCT00963560

Run by

Alcon Research

People needed

132

Starts

2009-08-01

Last updated by the study team

2011-08-09

Who can join

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

You may qualify if…

• diagnosed with bilateral cataracts
• candidate for presbyopic lens

You may not qualify if…

• > 1 Diopter preoperative astigmatism by Keratometry readings
• pre-existing conditions that could skew the results

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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