Status:
COMPLETED
A Comparison of Visual Function After Bilateral Implantation of Presbyopia-correcting Intraocular Lenses (IOLs)
Lead Sponsor:
Alcon Research
Conditions:
Cataract
Eligibility:
All Genders
21+ years
Phase:
PHASE4
Brief Summary
The purpose of this study is to prospectively evaluate postoperative visual and refractive parameters in a series of subjects bilaterally implanted with the AcrySof® IQ ReSTOR® +3 versus those bilater...
Eligibility Criteria
Inclusion
- diagnosed with bilateral cataracts
- candidate for presbyopic lens
Exclusion
- \>1 Diopter (D) preoperative astigmatism by Keratometry (K)readings
- pre-existing conditions that could skew the results
Key Trial Info
Start Date :
July 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
65 Patients enrolled
Trial Details
Trial ID
NCT01166971
Start Date
July 1 2010
Last Update
November 24 2011
Active Locations (3)
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1
The Eye Center of North Florida
Panama City, Florida, United States, 32405
2
Carolina Eye Care Physicians
Charleston, South Carolina, United States, 29414
3
Whitsett Vision Group
Houston, Texas, United States, 77055