Visual Function and Patient Satisfaction After Bilateral Implantation of AcrySof Natural ReSTOR (Model SN60D3) or AcrySof Natural Monofocal (Model SN60AT)
Completed · Not applicable
Conditions studied: Cataract
In brief
The purpose of the study is: * to compare visual parameters (Subjective refraction and Visual Acuity (VA)) and safety (tilt, decentration and posterior chamber opacification (PCO)) in a prospective series of 40 patients after bilateral implantation of AcrySof Natural ReSTOR (Model SN60D3) or AcrySof Natural Monofocal (Model SN60AT) * to assess patient satisfaction before and after implant
Key facts
- Study ID
- NCT00759668
- Run by
- Alcon Research
- People needed
- 35
- Starts
- 2007-05-01
- Expected to finish
- 2009-09-01
- Last updated by the study team
- 2011-01-26
Who can join
Age: 50 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Contact Alcon Call Center for Trial Locations — Fort Worth, Texas, United States
Full record on ClinicalTrials.gov
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