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Clinical Trial Summary

This study is a 6-month, prospective, multicenter, bilateral, randomized subject- and evaluator-masked, clinical investigation of the TECNIS Eyhance IOL versus the TECNIS 1-piece IOL. The study will be conducted at up to 15 sites in the U.S.A and will enroll approximately 220 subjects to achieve approximately 200 randomized and bilaterally implanted subjects, resulting in approximately 100 evaluable subjects in each lens group at 6 months. Subjects are to be implanted with the same IOL in both eyes: TECNIS Eyhance IOL or the TECNIS 1-Piece IOL. The eye implanted first will be considered the primary study eye.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05025345
Study type Interventional
Source Johnson & Johnson Surgical Vision, Inc.
Contact Study Contact
Phone +1 714 7218682
Email [email protected]
Status Recruiting
Phase N/A
Start date September 2, 2021
Completion date October 31, 2022

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