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Study identifier: NCT05561478 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Comparison of Visual Outcomes After Implantation of the Synthesis Plus and Synthesis Plus Toric

Condition: Cataract · Surgery · IOL  ·  Sponsor: Cutting Edge SAS

PhaseN/A
Planned participants72
Who can joinAll sexes, 50 Years to no upper limit
Healthy volunteersNo

About this study

Prospective controlled monocentric study to determine the non-inferiority of the distance-corrected intermediate visual acuity at 66 cm of the SYNTHESIS PLUS TORIC with respect to the SYNTHESIS PLUS IOL.

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

Talk to the study team

Line Bettinelli, OD  ·  0619530701  ·  line.bettinelli@cutting-edge.fr

Always discuss trial participation with your own doctor first.

Locations (1)

VISISPerpignan, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT05561478