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Study to Evaluate the Safety and Effectiveness of the enVista® Beyond (EY) EDF Intraocular Lens in Subjects Undergoing Cataract Extraction

Cataract Clinical Trial

Official title:
A Prospective, Multicenter, Randomized, Controlled Clinical Study to Evaluate the Safety and Effectiveness of the enVista® Beyond (EY) EDF Intraocular Lens in Subjects Undergoing Cataract Extraction

Clinical Trial Summary

This research study is evaluating the safety and efficacy (performance) of the Bausch + Lomb enVista Beyond Hydrophobic Acrylic Extended Depth of Focus Intraocular Lens (IOL) in subjects who receive this IOL in both eyes.

Clinical Trial Description

The study will evaluate the safety and effectiveness of the enVista Beyond (EY) EDF IOL in providing increased depth of focus, comparable distance and improved near and intermediate visual acuity compared to the parent enVista monofocal IOL. This is a prospective, multicenter, randomized, controlled, subject and visual acuity assessor masked, parallel-group study in subjects bilaterally implanted with either EY or TECNIS 1-Piece monofocal IOL following cataract surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06333015
Study type Interventional
Source Bausch & Lomb Incorporated
Contact Jenny Hledik
Phone 5033511248
Email Jenny.Hledik@bausch.com
Status Not yet recruiting
Phase N/A
Start date April 2024
Completion date October 2025
View Details
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