Myopia Clinical Trial - Clinical Trial With Artiflex Presbyopic

Status Recruiting

Clinical Trial Summary

The purpose of this clinical trial is to evaluate the effectiveness and safety of the multifocal Artiflex Presbyopic intraocular lens.

Clinical Trial Description

The study is a prospective, open-label, single-arm, and multicentre clinical investigation with three years of follow-up. Artiflex Presbyopic is a phakic intraocular lens to be implanted in the anterior chamber, intended for adult subjects and indicated for the optical correction of presbyopia and spherical error requiring a correction. The results of this study will be used for CE-approval and registration as well as marketing purposes. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04632784
Study type	Interventional
Source	Ophtec BV
Contact	Erwin Bouwman, MSc
Phone	+31 (0)6 83246222
Email	study@ophtec.com
Status	Recruiting
Phase	N/A
Start date	November 12, 2021
Completion date	July 2025

View Details

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