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Clinical Trial Summary

The objective of this study was to evaluate the clinical and patient reported outcomes after bilateral implantation of the AcrySof™ IQ Vivity™ Toric intraocular lens.


Clinical Trial Description

This is a prospective interventional case series of 30 patients who underwent cataract surgery and bilateral implantation of the AcrySof™ IQ Vivity™ Toric intraocular lens. This study is represented by an Asian cohort of patients and the study evaluations were focused not only on clinical visual outcomes but also on "real-life" patient reported outcomes such as dysphotopsias, spectacle independence and daily visual tasks all of which were measured at 1 month and up to 3 months postoperatively. The objective would be to provide insight into the performance of this intraocular lens in Asian patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06196593
Study type Interventional
Source LEC Eye Centre
Contact
Status Completed
Phase N/A
Start date April 1, 2022
Completion date April 30, 2023

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