Visual Function After Bilateral Implantation of AcrySof® Toric

Completed · Phase 4

Conditions studied: Visual Function

In brief

The objective of this study was to evaluate visual function of AcrySof Toric and AcrySof Natural Intraocular Lenses (IOLs) following implant for replacement of cataract.

Key facts

Study ID

NCT00758550

Run by

Alcon Research

People needed

60

Starts

2007-04-01

Last updated by the study team

2010-03-16

Who can join

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

You may qualify if…

• Bilateral cataracts
• 40\~80 years of age
• 4 Days - 1 Week interval between a single patient's surgery
• dilated pupil size (in dim light) ≥ 4.0 mm
• Anticipated correction with an IOL of +10 Diopters \~ +25 Diopters
• 0.75 - 2.0 Diopters of astigmatism preoperatively as measured by Keratometry readings

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(within 6 months prior to first surgery)

Where it is running

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

Full record on ClinicalTrials.gov

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