Visual Function After Implantation of Bilateral AcrySoft ReSTOR Aspheric IOL

Completed · Phase 4

Conditions studied: Cataract

In brief

This study will involve up to 20 bilateral patients per surgeon. Patients will be assessed pre-operatively, and at subsequent visits (following the implantation of the intraocular lens in the second eye) at 1 week, 1 month, 3 months and 6 months post-operatively.

Key facts

Study ID

NCT00934622

Run by

Alcon Research

People needed

76

Starts

2007-11-01

Last updated by the study team

2010-05-06

Who can join

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

You may qualify if…

• 21 years or older;
• need spherical correction between 10-30 Diopters (D);
• corneal astigmatism less than 0.75D as measured by keratometry;
• willing to sign an Informed Consent Form and complete all visits;
• pupil dilation greater than 6mm;
• expected Visual Acuity (measured in logMAR)=0.3 or better

You may not qualify if…

• Women of childbearing potential;
• irregular corneal astigmatism;
• keratopathy/keratectasia;
• cornea inflammation or edema;
• cornea reshaping surgery;
• corneal dystrophy;corneal transplant;
• amblyopia;
• glaucoma;
• Retinal Pigment Epitheliopathy (RPE)/Macular changes;
• proliferative diabetic retinopathy

Where it is running

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

Full record on ClinicalTrials.gov

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