Real-World Study of Vivity Intraocular Lenses (IOLs)

Status Withdrawn

Clinical Trial Summary

The primary objective of this clinical study is to assess the clinical performance of the AcrySof IQ Vivity Extended Vision IOL in a Chinese population.

Clinical Trial Description

In this clinical study, subjects will be implanted with the AcrySof IQ Vivity Extended Vision IOL in both eyes. The second eye surgery will occur 7-28 days after the first eye. A total of 11 scheduled visits are planned, including a screening visit, two operative visits, and 8 postoperative visits. The total expected duration of the subject's participation will be about 13 months. This study will be conducted in China. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04800016
Study type	Interventional
Source	Alcon Research
Contact
Status	Withdrawn
Phase	N/A
Start date	June 2021
Completion date	July 2024

View Details

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