Status:
COMPLETED
Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL
Lead Sponsor:
Alcon Research
Conditions:
Visual Acuity
Eligibility:
All Genders
21+ years
Phase:
NA
Brief Summary
The purpose of this study is to assess uniocular and binocular unaided distance, intermediate, and near VA; contrast sensitivity, accommodation amplitude, stereopsis, glare testing, ocular aberrations...
Eligibility Criteria
Inclusion
- ≥21 years of either gender or any race
- Potential post-op VA 20/20
- Pre-op astigmatism ≤ 1.0D
- Able to sign the informed consent
- Able to complete all required postoperative visits
- Planned cataract removal by phaco
- Clear intraocular media other than cataract
Exclusion
- Signs of capsular tear, significant anterior chamber hyphema, or zonular rupture
- Any corneal pathology and previous corneal refractive surgery
- Patients with unrealistic expectations in anticipated post-op VA
- Happy to wear glasses
- Occupational night driver
Key Trial Info
Start Date :
May 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2008
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT00759096
Start Date
May 1 2007
End Date
July 1 2008
Last Update
December 5 2023
Active Locations (1)
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1
Alcon Call Center
Fort Worth, Texas, United States, 76134