Rotational Stability of the AcrySof® Toric

Completed · Not applicable

Conditions studied: Cataract

In brief

To assess the rotational stability and the residual refractive cylinder and patient reported outcomes of the AcrySof Toric intraocular lens after unilateral or bilateral implantation.

Key facts

Study ID

NCT00762216

Run by

Alcon Research

People needed

71

Starts

2008-05-01

Last updated by the study team

2012-10-31

Who can join

Age: 40 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Monolateral or bilateral cataracts
• anticipated intraocular lens (IOL) power of +10 Diopters (D) \~ +25D
• 0.75 \~ 2.0 D of astigmatism measured preoperatively by Keratometry readings
• able to sign the informed consent, to comply with scheduled visits and other study procedures

You may not qualify if…

• Preoperative ocular pathology
• previous intraocular or corneal surgery
• an increased risk for complications which could require vitreoretinal surgery
• corneal irregularities
• corneal opacities
• current contact lens usage
• uncontrolled diabetes

Where it is running

• Alcon Call Center — Fort Worth, Texas, United States

Full record on ClinicalTrials.gov

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