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Clinical Trial Summary

The purpose of the study is to evaluate clinical and functional performance in real-world conditions in participants who have been implanted with Acrysof IQ Vivity (Extended Vision) IOLs compared with Alcon Aspheric Monofocal IOLs.


Clinical Trial Description

This observational study will enroll subjects who have been implanted with an Alcon aspheric monofocal or monofocal toric IOL no less than 4 months prior to study procedures. This study will be conducted in Australia. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05414565
Study type Observational
Source Alcon Research
Contact Jessie Hull, DrPH
Phone +1 817-909-6199
Email jessie.hull@alcon.com
Status Recruiting
Phase
Start date September 15, 2022
Completion date March 2024

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