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Evaluation of Quality of Vision and Spectacle Independence With the AcrySof® Panoptix® Intraocular Lens

Cataract Clinical Trial

Official title:
Evaluation of Quality of Vision and Spectacle Independence With Bilateral Implantation of the AcrySof® Panoptix® Intraocular Lens

Clinical Trial Summary

This is a study to assess the spectacle independence and quality of vision of patients receiving the AcrySof® Panoptix® Intraocular lens (IOL) after uneventful cataract surgery.

Clinical Trial Description

This study is a single-arm unmasked clinical evaluation study of spectacle independence after successful bilateral cataract surgery. Subjects will be assessed pre-operatively, operatively and at 1 day, 1 month and 3 months post-operatively. Clinical evaluations will include administration of a spectacle independence questionnaire, as well as measurement of bilateral visual acuity and manifest refraction. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04124952
Study type Observational
Source SightTrust Eye Institute
Contact
Status Completed
Phase
Start date October 3, 2019
Completion date February 16, 2021
View Details
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