Clinical Trials Directory

Trials / Completed

CompletedNCT05414565

Post-Market Study of Alcon Intraocular Lenses

Clinical and Functional Performance of Acrysof IQ Vivity Versus Aspheric Monofocal IOLs

Status
Completed
Phase
Study type
Observational
Enrollment
50 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
50 Years – 70 Years
Healthy volunteers
Accepted

Summary

The purpose of the study is to evaluate clinical and functional performance in real-world conditions in participants who have been implanted with Acrysof IQ Vivity (Extended Vision) IOLs compared with Alcon Aspheric Monofocal IOLs.

Detailed description

This observational study will enroll subjects who have been implanted with an Alcon aspheric monofocal or monofocal toric IOL no less than 4 months prior to study procedures. This study will be conducted in Australia.

Conditions

Interventions

TypeNameDescription
DEVICEVivity IOLCommercially available extended vision IOL
DEVICEAspheric monofocal IOLCommercially available aspheric IOL

Timeline

Start date
2022-09-15
Primary completion
2024-04-15
Completion
2024-04-15
First posted
2022-06-10
Last updated
2024-07-09

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT05414565. Inclusion in this directory is not an endorsement.