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Trifocal Intraocular Lens (IOL) Aberrometry Outcomes

NCT04196569 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 24

Last updated 2022-12-15

No results posted yet for this study

Summary

The goal of this study is to evaluate subject outcomes and spectacle independence with intraoperative aberrometry and trifocal IOL implantation.

Conditions

  • Cataract

Interventions

DEVICE

Alcon Trifocal and Trifocal Toric Intraocular Lenses

Panoptix Model #TFAT00 for the UV Absorbing Trifocal IOL. Torics: TFAT30, TFAT40, TFAT50, TFAT60

Sponsors & Collaborators

  • Alcon Research

    collaborator INDUSTRY

  • Weill Medical College of Cornell University

    lead OTHER

Principal Investigators

  • Ashley Brissette, MD · Weill Medical College of Cornell University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-12-12
Primary Completion
2022-09-13
Completion
2022-09-13

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 NCT04196569 on ClinicalTrials.gov