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Clinical Trial Summary

Cataract is characterized by the loss of the normal transparency of the crystalline lens. It is a progressive, chronic disease that affect individuals over the age of 50. It is the leading cause of blindness around the world. The EyenableTM IOL (PA60AS1) is a CE-marked foldable single-piece ultra-violet absorbing posterior chamber intraocular lens (IOL). It is an optical implant to replace the human crystalline lens in the visual correction of aphakia in adult patients after cataract removal. This post-market clinical study will investigate the implantation safety and performance of the EyenableTM PA60AS1 intraocular lens (IOL) up to 6 month after the surgery.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06223113
Study type Interventional
Source Xi'an Eyedeal Medical Technology Co., Ltd
Contact Q. Trin Peng, MD
Phone +86 029 848 88888
Email info@eyedeal.com
Status Not yet recruiting
Phase N/A
Start date February 2024
Completion date February 2025

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