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Clinical Trial Summary

The objective is to assess the visual outcomes and quality of vision of patients receiving the AcrySof® Vivity Intraocular lens (IOL), when implanted in eyes with high ocular axial length (≥24.5mm), after uneventful cataract surgery.


Clinical Trial Description

This study is a single-arm unmasked clinical evaluation study of binocular uncorrected visual acuity at distance (6m), intermediate (66cm) and near (40cm), when implanted in eyes with high ocular axial length (≥24.5mm), after successful bilateral cataract surgery. Subjects will be assessed preoperatively, operatively, and at 1 day, 1 week, 1 month, and 3 months postoperatively. Clinical evaluations will include administration of a visual disturbance questionnaire (QUVID) and a satisfaction questionnaire (IOLSAT), as well as measurement of binocular and monocular visual acuities and manifest refraction. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05210569
Study type Observational
Source Dr. James J. Wiens Medical Corporation
Contact Lori Groening
Phone 204-943-1520
Email [email protected]
Status Recruiting
Phase
Start date January 13, 2022
Completion date October 15, 2022

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