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Clinical Trial Summary

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


Clinical Trial Description

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


Study Design


Related Conditions & MeSH terms


NCT number NCT06258707
Study type Interventional
Source Cutting Edge SAS
Contact Ilham XHAARD
Phone 620 050 651
Email ilham.xhaard@cutting-edge.fr
Status Not yet recruiting
Phase N/A
Start date April 15, 2024
Completion date January 15, 2026

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