VIS Opti-K Vision Improvement for Presbyopes

NCT06702020 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 135

Last updated 2024-11-22

No results posted yet for this study

Summary

The VIS Opti-K device and procedure were used to provide vision improvement to patients with presbyopia.

Conditions

  • Presbyopia Correction

Sponsors & Collaborators

  • VIS, Inc.

    lead INDUSTRY

Principal Investigators

  • Michael J Berry, PhD · VIS, Inc.

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-03-13
Primary Completion
2025-03-31
Completion
2025-07-31

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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 NCT06702020 on ClinicalTrials.gov