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Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness and safety of the TFNT20 low cylinder power intraocular lens when implanted in the eye to replace the natural lens following cataract removal.


Clinical Trial Description

Subjects will attend a total of 5 to 9 visits, depending on whether one eye or both eyes are implanted. The second eye surgery, if applicable, will occur 1 to 30 days after the first eye surgery. Total individual duration of participation will be up to 4 months, including an up to 2-month preoperative period. This study will be conducted in Japan. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04542525
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date December 1, 2020
Completion date August 10, 2021

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