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Trials / Completed

CompletedNCT04954898

Post-market Evaluation of Clinical Outcomes in China for the TECNIS Model ZMT

Post-market Evaluation of Clinical Outcomes in China for the TECNIS® Multifocal Toric 1-Piece Intraocular Lens Model Series ZMT

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
102 (actual)
Sponsor
Johnson & Johnson Surgical Vision, Inc. · Industry
Sex
All
Age
22 Years
Healthy volunteers
Not accepted

Summary

This is a prospective, multicenter, single-arm, open-label clinical study of the commercially available TECNIS Multifocal Toric 1-Piece IOL. The study will enroll up to 120 subjects from up to 8 sites in China. The subjects will be followed for 12-months postoperatively.

Conditions

Interventions

TypeNameDescription
DEVICEStudy Lens: TECNIS Multifocal Toric 1-piece lens, Model ZMTSurgeons will perform standardized, small-incision, cataract surgery and implant the study lenses using a JJSV-validated insertion system qualified for use with TECNIS Multifocal Toric 1-Piece IOL.

Timeline

Start date
2021-08-11
Primary completion
2024-01-10
Completion
2024-01-10
First posted
2021-07-08
Last updated
2025-05-23

Locations

7 sites across 1 country: China

Source: ClinicalTrials.gov record NCT04954898. Inclusion in this directory is not an endorsement.

Post-market Evaluation of Clinical Outcomes in China for the TECNIS Model ZMT (NCT04954898) · Clinical Trials Directory