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Clinical Trial Summary

The objective of this study is to obtain an initial assessment of the safety and performance of an investigational AIOL in patients undergoing cataract extraction and IOL implantation.


Clinical Trial Description

This study was originally designed as a single arm, unilateral study (one eye, one product only) to obtain an initial assessment of the safety and performance of an investigational IOL in subjects undergoing cataract extraction and IOL implantation. The study design was later modified to a contralateral study (both eyes, different product in each eye) to compare the safety and performance of the investigational IOL to a commercially available monofocal IOL. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03925545
Study type Interventional
Source PowerVision
Contact
Status Completed
Phase N/A
Start date January 17, 2017
Completion date November 27, 2018

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