NCT06258707View on ClinicalTrials.gov

Bicentric Clinical Investigation to Assess Safety and Performance of LuxBoost IOL

NARecruitingINTERVENTIONAL
Enrollment

58

Participants

Timeline

Start Date

October 14, 2024

Primary Completion Date

September 15, 2026

Study Completion Date

December 15, 2026

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.

Trial Locations (2)

35000

RECRUITING

West Optha, Rennes

82000

RECRUITING

Clinique Honore Cave, Montauban

All Listed Sponsors
lead

Cutting Edge SAS

INDUSTRY