Comparison of Corneal Aberrations and Visual Outcomes in AcrySof IQ Toric Patients Versus Limbal Relaxing Incision (LRI) Patients

Withdrawn before enrolling · Phase 4

Conditions studied: Cataracts

In brief

A prospective evaluation of postoperative corneal aberrations and visual parameters in patients assigned to either an AcrySof IQ Toric intraocular lens (IOL) group or a group implanted with a SN60WF IOL and having concomitant limbal relaxing incision.

Key facts

Study ID

NCT00929747

Run by

Alcon Research

People needed

0

Starts

2009-06-01

Expected to finish

2009-10-01

Last updated by the study team

2012-04-12

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• operable cataracts
• good ocular health
• 0.5 D to 2.0 D of corneal astigmatism

You may not qualify if…

• > 2.0 D astigmatism
• irregular astigmatism
• prior or ongoing corneal disease or scarring
• history of ocular disease

Where it is running

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

Full record on ClinicalTrials.gov

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