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Clinical Investigation of the Visual Outcomes and Safety of a Trifocal Toric IOL in an Asian Population

Aphakia Clinical Trial

Official title:
Clinical Investigation of the Visual Outcomes and Safety of AcrySof® IQ PanOptix® Toric Trifocal IOLs in an Asian Population

Clinical Trial Summary

The purpose of this study is to evaluate the clinical performance of the ACRYSOF® IQ PanOptix® Toric Trifocal intraocular lens (IOL) when implanted in the eye following cataract removal in an Asian population.

Clinical Trial Description

Both eyes will be implanted with the PanOptix Toric Trifocal IOL. The eye with the highest astigmatism will be implanted first. The second eye will be implanted within 7-14 days of the first eye. Subjects will attend a total of 10 scheduled visits as follows: 1 screening visit, 1 operative visit for each eye, 2 post-operative visits for each eye, and 3 postoperative visits where both eyes will be evaluated. The duration of participation for each subject will be approximately 8 months. This study will be conducted in Australia. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04528069
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date November 16, 2020
Completion date December 17, 2021
View Details
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