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Patient Preference and Visual Quality With Contralateral Synergy Versus Panoptix

NCT05610540 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2023-07-27

No results posted yet for this study

Summary

The goal of this study is to compare the visual quality and patient preference of the Synergy IOL versus the PanOptix IOL when one of each lens is placed in the same patient.

Conditions

  • IOL
  • Cataract
  • Patient Satisfaction

Interventions

DEVICE

TECNIS Synergy IOL

Implanted in one eye

DEVICE

AcrySof PanOptix Trifocal IOL

Implanted in one eye

Sponsors & Collaborators

  • Bucci Laser Vision Institute

    lead OTHER

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-04-12
Primary Completion
2023-02-21
Completion
2023-05-31
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 NCT05610540 on ClinicalTrials.gov