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.
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.
Study Type
OBSERVATIONAL
Enrollment
50
Commercially available extended vision IOL
Commercially available aspheric IOL
School of Optometry and Vision Science, Queensland University of Technology
Kelvin Grove, Queensland, Australia
Binocular photopic best-corrected distance visual acuity (BCDVA)
Visual acuity will be measured using a standard visual acuity chart at a distance of 4 meters under photopic (well-lit) conditions and reported in logarithm Minimum Angle of Resolution (logMAR) units. Visual acuity will be measured binocularly (both eyes together).
Time frame: At least 4 months post-operative
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