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 group, patients receive a toric IOL according to their preoperative astigmatism
Condition | Age Related Cataracts, Astigmatism |
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Treatment | Intraocular lens implantation |
Clinical Study Identifier | NCT03803852 |
Sponsor | Medical University of Vienna |
Last Modified on | 27 May 2022 |
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