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A Comparative Study of TECNIS Symfony Plus IOL and a Trifocal IOL

Cataract Clinical Trial

Official title:
A Comparative Clinical Evaluation of a New TECNIS® Presbyopia-correcting Intraocular Lens Against a Trifocal Intraocular Lens

Clinical Trial Summary

This is a multicenter, prospective, randomized, subject- and evaluator-masked, bilateral-implant study conducted at up to 15 sites worldwide. A total of up to 280 subjects will be randomized in a 1:1 ratio for implantation with either the TECNIS Symfony plus IOL Model ZHR00V or the Trifocal IOL. This will ensure that data from at least 100 subjects in the TECNIS Symfony plus lens group and at least 100 subjects in the Trifocal lens group will be available for analysis at the 6-month follow-up timepoint. All subjects will be followed for up to 6 months postoperative.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04156737
Study type Interventional
Source Johnson & Johnson Surgical Vision, Inc.
Contact
Status Completed
Phase N/A
Start date January 24, 2020
Completion date July 14, 2021
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