Visual Performance of the Vivity IOL in Post-myopic LASIK and PRK Patients

NCT05961046 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 6

Last updated 2024-06-17

No results posted yet for this study

Summary

The objective is to evaluate visual outcomes and patient satisfaction in patients with a history of myopic LASIK or PRK who will have completed cataract surgery with the Vivity IOL.

Conditions

  • Cataract

Interventions

DEVICE

Vivity IOL

Vivity IOL

Sponsors & Collaborators

  • Sengi

    collaborator INDUSTRY
  • Laser & Corneal Surgery Associates

    lead OTHER

Principal Investigators

  • Jimmy Y Hu, MD · Laser and Corneal Surgery Associates

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-17
Primary Completion
2024-06-13
Completion
2024-06-13
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 NCT05961046 on ClinicalTrials.gov