Visual Outcome and Visual Quality After Bilateral Implantation of the AcrySof® IQ IOL Compared to MI60® and Tecnis® IOL

Withdrawn before enrolling · Phase 4

Conditions studied: Cataract

In brief

The objective of the study is to compare the visual outcomes of three aspheric monofocal intraocular lenses after cataract surgery - ACRYSOF® IQ, Tecnis® and Akreos® MI60.

Key facts

Study ID

NCT00760058

Run by

Alcon Research

People needed

0

Starts

2008-06-01

Expected to finish

2010-12-01

Last updated by the study team

2015-05-12

Who can join

Age: 50 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female subjects, aged 50 and over.
• Subjects diagnosed with bilateral cataracts requiring cataract extraction and implantation of a posterior chamber intraocular lens.
• Subjects must be willing to undertake the additional ophthalmic tests within 3 months of the second lens implantation.
• Subjects must be assessed to be able to dilate to a minimum of 6 mm pre operatively.
• Subjects' pupil size must be ≥ 4.5 mm in mesopic conditions.

You may not qualify if…

• Subjects who have previously had corneal surgery.
• Subjects who have potential visual acuity which is < 6/12 due to other ocular pathology
• Subjects with corneal pathology.
• Subjects with astigmatism of greater than 1D.
• Subjects diagnosed with glaucoma.
• Subjects diagnosed with diabetes.
• Subjects who have previously participated in a clinical investigation within 30 days prior to enrolment
• Subjects with a know history of poor compliance
• Subjects with planned adjunctive surgery

Where it is running

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

Full record on ClinicalTrials.gov

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