Clinical Trial

Unity VCS: A Comparison Study Evaluating Corneal Clarity and Thickness

Recruiting
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Record status
This record was last updated October 29, 2025 (before its estimated April 2026 completion). Its status may not reflect the trial's current state.
Summary
Phacoemulsification (cataract surgery) is usually performed while temporarily increasing the pressure inside the eye. The purpose of this study is to see if maintaining different pressure levels inside the eye during this procedure results in fewer side effects and better vision shortly after the surgery. Cataract surgery will be performed using Unity VCS at a lower IOP in one eye compared to traditional IOP with Centurion Vision System with Ozil in the other eye. Both of which are approved by the United States Food and Drug Administration (FDA) and used per label.
Trial Details
NCT Number NCT07222150
Lead Sponsor Metrolina Eye Associates, PLLC
Collaborators: Alcon, a Novartis Company
Conditions Cataract
Enrollment 105 participants
Start Date 2025-10-07
Primary Completion 2026-04 (estimated)
Study Completion 2026-10 (estimated)
Updated on ClinicalTrials.gov 2025-10-29