MedTrace Logo

Bicentric Clinical Investigation to Assess Safety and Performance of LuxBoost IOL

NCT06258707 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 58

Last updated 2026-02-12

No results posted yet for this study

Summary

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

Conditions

  • Aphakia

Interventions

DEVICE

LuxBoost IOL

Bilateral implantation in the capsular bag to replace the cataractous human crystalline lens.

DEVICE

LuxGood IOL

Bilateral implantation in the capsular bag to replace the cataractous human crystalline lens.

Sponsors & Collaborators

  • Cutting Edge SAS

    lead INDUSTRY

Principal Investigators

  • Vincent GUALINO · Clinique Honoré Cave 82000 Montauban

  • Christophe CESSES · Cutting Edge S.A.S (Sponsor)

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-10-14
Primary Completion
2026-12-15
Completion
2027-06-15

Countries

  • France

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06258707 on ClinicalTrials.gov