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Clareon PanOptix Pro vs. Clareon PanOptix - Study A

Presbyopia Clinical Trial

Official title:
Contralateral Study of Clareon PanOptix Pro vs. Clareon PanOptix

Clinical Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of Clareon™ PanOptix™ Pro Trifocal Intraocular Lens (IOL) compared to Clareon™ PanOptix™ Trifocal IOL.

Clinical Trial Description

Subjects will attend 9 scheduled study visits for a total individual duration of participation of approximately 7 months. The primary endpoint will be assessed at the Month 2 follow-up visit. Both eyes of a subject must qualify for enrollment into this study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06400745
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 June 18, 2024
Completion date July 2025
View Details
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