60
Participants
Start Date
January 1, 2023
Primary Completion Date
June 30, 2025
Study Completion Date
June 30, 2025
No intervention is subject of the study. Only standard pre- and postoperative data will be evaluated.
No intervention is subject of the study. Only standard pre- and postoperative data will be evaluated. Including data from testing refraction, visual acuity, biometry, tomography, and OCT.
IROC, Zurich
AMO Ireland
UNKNOWN
IROC AG
OTHER