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Clinical Evaluation of the FluidVision Accommodating Intraocular Lens (AIOL)

Aphakia Clinical Trial

Official title:
Clinical Evaluation of the FluidVision Accommodating Intraocular Lens

Clinical Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of an investigational IOL.

Clinical Trial Description

Eligible subjects will receive the investigational IOL in one eye and be followed at 1 day, 1 week, 1 month, 3 months, 6 months, 12 months, 18 months, 24 months and 36 months post-operation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02049567
Study type Interventional
Source PowerVision
Contact
Status Completed
Phase N/A
Start date January 14, 2014
Completion date November 6, 2017
View Details
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