Status:
WITHDRAWN
Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL
Lead Sponsor:
Alcon Research
Conditions:
Visual Outcomes
Eligibility:
All Genders
21+ years
Phase:
PHASE4
Brief Summary
An unmasked trial after bilateral implantation of AcrySof® ReSTOR®, SA60D3 IOL . Enrolled are at least 30 patients or as much as possible from the doctor's clinical practice perspective. 6 months foll...
Eligibility Criteria
Inclusion
- Able to complete all required postoperative visits; Planned cataract removal by phaco; 21 years of age or older, either gender or any race; potential postoperative visual acuity of 20/20; astigmatism ≦1.0D measured by keratometry in study eye(s);clear int
Exclusion
- Signs of capsular tear, significant anterior chamber hyphema;zonular rupture; corneal pathology and refractive surgery;hypercritical patient; patients with unrealistic expectations in post-op VA; happy to wear glasses;occupational night drivers
Key Trial Info
Start Date :
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00758940
Last Update
May 12 2015
Active Locations (1)
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1
Alcon Call Center
Fort Worth, Texas, United States, 76134