MedTrace Logo

This Clinical Trial Compares Two Phacoemulsification Systems Used in a Bilateral Cataract Surgery Subjects in Order to Study CDE and Ultrasound Time During Cataract Removal

NCT07468877 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-03-18

No results posted yet for this study

Summary

This clinical trial compares two phacoemulsification systems used in a bilateral cataract surgery subjects, in order to study CDE and Ultrasound time during cataract removal

Conditions

  • Nuclear Sclerosis of the Lens
  • Phacoemulsification Cataract Surgery
  • Cataract Bilateral

Interventions

DEVICE

Cataract extraction with phacoemulsification comparing two systems

First arm: Phacoemulsification using UNITY VCS/CS system with UNITY 4D phaco handpiece

DEVICE

Cataract extraction with phacoemulsification comparing two systems

Second arm: Phacoemulsification using Centurion system with OZil technology

Sponsors & Collaborators

  • Nicole Fram M.D.

    lead OTHER

Principal Investigators

  • Nicole R Fram, M.D. · Advanced Vision Care

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-02-13
Primary Completion
2027-02-13
Completion
2027-02-13
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT07468877 on ClinicalTrials.gov