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Clinical Trial Summary

The primary study objective is to compare the effectiveness of the combination of phacoemulsification with intraocular lens implant with ELIOS or competitor device in reducing IOP at 12 months postoperatively.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06246136
Study type Interventional
Source Elios Vision, Inc.
Contact Amandine Jacques
Phone +33670612439
Email amandine@eliosvision.com
Status Recruiting
Phase N/A
Start date December 5, 2023
Completion date June 30, 2026

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