Recommendations for Monitoring Clinical Experience Following Implantation of the AcrySof® Toric

Withdrawn before enrolling · Phase 4

Conditions studied: Cataract

In brief

To allow surgeons to obtain clinical experience on the postoperative uncorrected and best distance corrected visual acuities (UCVA and BDCVA) and corneal and refractive cylinder of the AcrySof Toric IOL.

Key facts

Study ID

NCT00761488

Run by

Alcon Research

People needed

0

Last updated by the study team

2015-05-12

Who can join

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

You may qualify if…

• 40-80 years old; of any race and gender; diagnosed with bilateral cataracts; require cataract extraction followed by implantation of a posterior chamber IOL; patients have between 0.75 -2.5 D of astigmatism preoperatively as measured by K readings.

You may not qualify if…

• Females of child bearing potential;irregular corneal astigmatism;keratopathy/Keratectasia; cornea inflammation or edema;previous corneal reshaping,dystrophy or transplant;amblyopia;glaucoma;RPE/Macular changes;diabetic retinopathy.

Where it is running

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

Full record on ClinicalTrials.gov

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