ACRYSOF® ReSTOR® Aspheric +3.0 D Add Power Intraocular Lens (IOL)
Completed · Phase 4
Conditions studied: Cataract
In brief
Randomized, parallel group, subject masked, multi-center six (6) month follow-up study comparing ACRYSOF® ReSTOR® Aspheric +3.0 D Add Power IOL Model SN6AD1 implanted in both eyes to ACRYSOF® ReSTOR® Aspheric +4.0 D Add Power IOL Model SN6AD3 implanted in both eyes.
Key facts
- Study ID
- NCT00684138
- Run by
- Alcon Research
- People needed
- 300
- Starts
- 2007-06-01
- Expected to finish
- 2008-06-01
- Last updated by the study team
- 2010-07-13
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Call Center for Locations — Fort Worth, Texas, United States
Full record on ClinicalTrials.gov
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