● Recruiting

Bicentric Clinical Investigation to Assess Safety and Performance of LuxBoost IOL

Condition: Aphakia · Sponsor: Cutting Edge SAS

PhaseNA

Planned participants58

Who can joinAll sexes, 50 Years to no upper limit

Healthy volunteersNo

About this study

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

This description comes directly from the study's public registry record.

Talk to the study team

Ilham XHAARD · 620 050 651 · ilham.xhaard@cutting-edge.fr

Line BETTINELLI · 619 530 701 · line.bettinelli@cutting-edge.fr

Always discuss trial participation with your own doctor first.

Locations (2)

Clinique Honore Cave	Montauban, France	Recruiting
West Ophta	Rennes, France	Recruiting

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Source record: clinicaltrials.gov/study/NCT06258707