Clinical Trials Directory

Trials / Completed

CompletedNCT02219997

Functional Vision With ACRYSOF® IQ IOLs Blue Light Filtration

Functional Benefit With ACRYSOF® Natural Chromophore

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Alcon Research · Industry
Sex
All
Age
65 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the reaction time (as measured by braking reaction time in seconds during simulated driving) under glare and no-glare conditions in subjects implanted with ACRYSOF® IQ intraocular lenses (IOLs) to subjects implanted with clear IOLs. This study will enroll subjects previously implanted with IOLs in both eyes for at least 3 months.

Detailed description

Subjects completed 2 visits to the investigational site.

Conditions

Interventions

TypeNameDescription
DEVICEClear clip-on glassesClip-on glasses with no blue light filtering properties used as a placebo
DEVICEBlue light filter clip-on glassesClip-on glasses with blue light filtering properties similar to ACRYSOF® IOLs
DEVICEACRYSOF® IQ IOLAcrySof IQ Aspheric Natural IOL Model SN60WF with UV and blue light filtering properties, previously implanted
DEVICEClear IOLClear IOL, previously implanted

Timeline

Start date
2014-10-01
Primary completion
2015-03-01
Completion
2015-03-01
First posted
2014-08-19
Last updated
2016-05-26
Results posted
2016-05-26

Source: ClinicalTrials.gov record NCT02219997. Inclusion in this directory is not an endorsement.