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Clinical Trial Summary

The investigational devices are approved intraocular lenses (IOL) intended to be implanted after phacoemulsification in individuals suffering from age-related cataract with the need of cataract surgery. Within the study, three different IOLs will be investigated and separately evaluated. Cataract surgery with IOL implantation will be performed in subjects who have signed an informed consent form. Postoperative examinations will be postoperative refraction, visual acuity, slitlamp examination, and rotation of the IOL within 1 hour, 1 week, 1 month and 4-7 months. In the Alcon Clareon toric and RayOne EMV toric groups, patients receive a toric IOL according to their preoperative astigmatism


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03803852
Study type Interventional
Source Medical University of Vienna
Contact Rupert Menapace, Prof.Dr.
Phone 0043-1-40400
Email rupert.menapace@meduniwien.ac.at
Status Recruiting
Phase N/A
Start date January 21, 2019
Completion date October 14, 2024

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