Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL
Phase 4
Withdrawn
- Conditions
- Visual Outcomes
- Interventions
- Device: Acrysof ReSTOR multifocal IOL
- Registration Number
- NCT00758940
- Lead Sponsor
- Alcon Research
- 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 follow-up after IOL implant in the 2nd eye
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- 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 Criteria
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description 1 Acrysof ReSTOR multifocal IOL Acrysof ReSTOR multifocal IOL
- Primary Outcome Measures
Name Time Method Near,intermediate,distance visual acuity pre-op;1 week after 1st eye surgery,1month and 6 month after 2nd eye surgery
- Secondary Outcome Measures
Name Time Method contrast sensitivity 6 month after 2nd eye surgery
Trial Locations
- Locations (1)
Alcon Call Center
🇺🇸Fort Worth, Texas, United States