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Clinical Trial Summary

This objective of this study is to evaluate the safety, and to collect supportive data on effectiveness of the EVO/EVO+ Visian® Implantable Collamer® Lens (ICL) in study participants who have a diagnosis of myopia or myopia with astigmatism. Primary study analysis will be evaluated when 300 primary eyes complete 6 months of follow-up. Final study analysis will be assessed when all treated eyes complete 36 months of follow-up.


Clinical Trial Description

This study will be conducted at up to 20 clinical sites in the United States by surgeons qualified by training and experience to implant STAAR ICLs. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04283149
Study type Interventional
Source Staar Surgical Company
Contact
Status Completed
Phase N/A
Start date January 30, 2020
Completion date December 15, 2023

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