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Clinical Trial Summary

The purpose of this post-market study is to describe the long-term safety and performance of Clareon Toric Intraocular Lenses (IOLs).


Clinical Trial Description

Subjects will attend up to 12 scheduled visits (one preoperative visit, up to two surgical visits, and up to 9 postoperative visits) over the course of the study (3 years follow-up). The overall study duration is expected to be approximately 4 years. This study will be conducted in Canada. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06285695
Study type Interventional
Source Alcon Research
Contact Alcon Call Center
Phone 1-888-451-3937
Email alcon.medinfo@alcon.com
Status Recruiting
Phase N/A
Start date April 4, 2024
Completion date April 2028

See also
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