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Effect of Intraocular Lens (IOL) Centration and Tilt on Visual Performance With Clareon® Vivity® IOL Implantation

NCT05827133 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 101

Last updated 2024-08-28

No results posted yet for this study

Summary

The goal of this observational study is to assess the effect of intraocular lens (IOL) movement in patients who have undergone Clareon® Vivity® IOL implantation.

The main question it aims to answer is: Does an association exist between IOL movement and patient quality of vision?

Participants implanted with Clareon® Vivity® and Vivity® Toric IOLs will be asked to do the following:

* consent to participate in the study
* allow researchers to access their personal medical records
* undergo a series of tests to assess the position of their IOLs and quality of vision

Researchers will assess participant examination results to determine whether an association exists between IOL movement and patient quality of vision.

Conditions

  • Cataract
  • Lenses, Intraocular

Interventions

OTHER

No intervention

No intervention

Sponsors & Collaborators

  • Alcon Research

    collaborator INDUSTRY

  • Florida Eye Specialists

    collaborator UNKNOWN

  • East Coast Institute for Research

    lead NETWORK

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-07-10
Primary Completion
2024-07-23
Completion
2024-07-23
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 NCT05827133 on ClinicalTrials.gov