Status:
WITHDRAWN
Visual Outcome and Visual Quality After Bilateral Implantation of the AcrySof® IQ IOL Compared to MI60® and Tecnis® IOL
Lead Sponsor:
Alcon Research
Conditions:
Cataract
Eligibility:
All Genders
50+ years
Phase:
PHASE4
Brief Summary
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.
Eligibility Criteria
Inclusion
- 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.
Exclusion
- 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
Key Trial Info
Start Date :
June 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2010
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00760058
Start Date
June 1 2008
End Date
December 1 2010
Last Update
May 12 2015
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Alcon Call Center
Fort Worth, Texas, United States, 76134