Clinical Investigation of the Multifocal IOL POD F GF in Cataracteous Eyes

Status Completed

Clinical Trial Summary

To evaluate effectiveness and safety of the POD F GF Intraocular Lens (IOL) when implanted to replace the natural lens following cataract removal

Clinical Trial Description

Since the investigational lens, like conventional IOLs, is a posterior chamber lens which is widely implanted following cataract extraction, phacoemulsification is adopted. To assess the binocular vision, the investigational lens will be bilaterally implanted. Considering the safety of the study subjects, the time of implant to the remaining eye (2nd eye) will be decided based on the results of the 1st implant. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04699266
Study type	Interventional
Source	Beaver-Visitec International, Inc.
Contact
Status	Completed
Phase	N/A
Start date	November 1, 2020
Completion date	August 30, 2021

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