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Clinical Trial Summary

The primary purpose of this study is to compare the Clareon/Clareon Toric Intraocular Lenses (IOLs) to the Eyhance/Eyhance Toric IOLs in binocular Best Corrected Distance Visual Acuity (BCDVA) at 3 months postoperative.


Clinical Trial Description

This study will enroll adults 22 years of age and older diagnosed with cataracts in both eyes with planned bilateral cataract removal by routine small incision phacoemulsification surgery. Subjects will attend up to 7 scheduled visits: A screening visit, two operative visits, and four post-operative visits. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05481125
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date October 10, 2022
Completion date October 16, 2023

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