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Clinical Investigation of the AcrySof IQ Vivity Extended Vision Intraocular Lens (IOL)

Aphakia Clinical Trial

Official title:
A Prospective, Randomized, Controlled, Multi-Center Clinical Investigation of the AcrySof IQ Vivity Extended Vision IOL vs. TECNIS Symfony and AT LARA Extended Depth of Focus IOLs

Clinical Trial Summary

The purpose of this study is to compare the visual disturbance profile of an intraocular lens (IOL) using nondiffractive optics, the VIVITY IOL, to two diffractive IOLs in subjects requiring bilateral cataract surgery. IOLs are implantable medical devices intended for long-term use over the lifetime of the cataract patient.

Clinical Trial Description

A total of 10 scheduled visits are planned. The visits include a screening visit, 2 operative visits, and 7 postoperative visits. Both eyes will be implanted. The second eye implant will occur within 7-21 days of the first eye implant. The primary endpoint data will be collected at the Month 3 visit. Individual subject participation is expected to last 6-7 months. This study will be conducted in Australia and New Zealand. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04098367
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date November 18, 2019
Completion date July 22, 2021
View Details
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