Unity VCS: A Comparison Study Evaluating Corneal Clarity and Thickness at Day 1 and Day 8 Post Op

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Cataracts

Locations
United States
North Carolina
Metrolina Eye Associates
RECRUITING
Matthews
Contact Information
Primary
IVAN MAC, MD
imac@metrolinaeye.com
7042341930
Backup
Megan Lee
mlee@metrolinaeye.com
7042341930
Time Frame
Start Date: 2025-10-07
Estimated Completion Date: 2026-10
Participants
Target number of participants: 105
Treatments
Active_comparator: Unity VCS
Cataract surgery with Unity VCS
Active_comparator: Centurion with Ozil
Cataract surgery with Centurion with Ozil
Related Therapeutic Areas
Sponsors
Leads: Metrolina Eye Associates, PLLC
Collaborators: Alcon, a Novartis Company

This content was sourced from clinicaltrials.gov