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Clinical Trial Summary

This study seeks to generate clinical data from subjects previously implanted with the Clareon Vivity/Clareon Vivity Toric IOLs or Clareon Monofocal/Clareon Toric IOLs. This study will assess key performance endpoints to support clinical benefits with model-specific data.


Clinical Trial Description

Both eyes of a subject must qualify for enrollment into this study. A total of 2 scheduled visits are planned. The visits include a Screening visit (Visit 0) and a visit after screening (Visit 1). Visit 1 should occur 1 to 14 days after Visit 0. Subject participation is expected to last approximately 2 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05852470
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date May 23, 2023
Completion date October 27, 2023

See also
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