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Clinical Trial Summary

The purpose of this research is to assess the rotational stability of the AcrySof IQ Vivity Extended Vision Toric IOL and Refractive Visual outcome.


Clinical Trial Description

Assessment of the rotational stability and Refractive Visual Outcome of the AcrySof IQ Vivity Extended Vision Toric IOL at the end of surgery, post op 1 day, post op 1 week and post op 4 weeks. Participants in this research study are 45 years of age or older and have planned implantation in at least one eye. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05119127
Study type Interventional
Source Central Florida Eye Specialists, LLC
Contact
Status Completed
Phase N/A
Start date September 30, 2020
Completion date August 19, 2021

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