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Post-Approval Study of the TECNIS SYMFONY® Toric Lenses

NCT03791619 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 475

Last updated 2023-08-29

Study results available
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Summary

This study is a prospective, multicenter, bilateral, non-randomized, open-label, comparative, 6-month clinical study conducted at up to 50 sites in the USA.

Conditions

  • Cataract
  • Corneal Astigmatism

Interventions

DEVICE

Higher Cylinder Toric IOL

Symfony Toric models ZXT300 and ZXT375 IOL

DEVICE

Lower Cylinder Toric IOL

Symfony Toric model ZXT150 IOL

Sponsors & Collaborators

  • Johnson & Johnson Surgical Vision, Inc.

    lead INDUSTRY

Principal Investigators

  • Johnson & Johnson Surgical Vision Clinical Trials · Johnson & Johnson Surgical Vision

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-12-13
Primary Completion
2022-08-08
Completion
2022-08-08
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03791619 on ClinicalTrials.gov