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Clinical Trial Summary

This will be a prospective, open-label, 125 subject (maximum), two-year multicentre investigation to assess the safety, effectiveness and rotational stability of the modified 600C (axis marks) intraocular lens (IOL) in subjects undergoing cataract extraction.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02378636
Study type Interventional
Source Rayner Intraocular Lenses Limited
Contact
Status Withdrawn
Phase N/A
Start date June 2015
Completion date August 2017

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