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Clinical Trial Summary

The study purpose is to demonstrate safety and performance of bilateral implantation of LuxHighAdd intraocular lens compared with the LuxGood Monofocal lens.


Clinical Trial Description

The study purpose is to demonstrate safety and performance after bilateral implantation of LuxHighAdd intraocular lenses. The device under investigation is a hydrophobic acrylic multifocal intraocular lens (IOL) manufactured by the sponsor of this study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06446817
Study type Interventional
Source Cutting Edge SAS
Contact Line Bettinelli, OD
Phone 0619530701
Email line.bettinelli@cutting-edge.fr
Status Not yet recruiting
Phase N/A
Start date September 1, 2024
Completion date July 1, 2026

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