Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT07222150 · ClinicalTrials.gov registry record · NA
Unity VCS: A Comparison Study Evaluating Corneal Clarity and Thickness
A NA study of Cataract, sponsored by Metrolina Eye Associates, P.
- Recruiting
- Registry status
- NA
- Development phase
- 105
- Enrollment target
- 1
- Study location
NCT07222150: Recruiting NA study of Cataract, sponsored by Metrolina Eye Associates, P.
NCT07222150 is a NA study of Cataract that is actively recruiting participants, run by Metrolina Eye Associates, P. The registered enrollment target is 105 participants, below the 227-participant average among 83 other Cataract trials with a reported enrollment target (54% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07222150, a NA study of Cataract, is actively recruiting participants, sponsored by Metrolina Eye Associates, P.
- RECRUITING
- Registry status
- NA
- Development phase
- 105 participants
- Enrollment target
- 1
- Study location
Study 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.
Primary Outcome
Measurement of post-operative CCT pre and post-operatively with Pentacam
Conditions Studied
Interventions
- DEVICE Cataract surgery with Unity VCS
- DEVICE Cataract surgery with Centurion with Ozil
Study Locations (1)
North Carolina
- Metrolina Eye Associates - Matthews
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 105 participants |
| Start Date | 2025-10-07 |
| Est. Completion | 2026-10 |
| Phase | NA |
What NCT07222150 shows while recruiting
NCT07222150 is an interventional study that assigns participants to a tested intervention. The registered 105 participants enrollment target is mid-sized for trials with a published cap, below the 227-participant average among 83 other Cataract trials with a reported enrollment target (54% lower).
The record links to 1 condition, with Cataract appearing as the primary indexed condition, and to 2 interventions - of which Cataract surgery with Unity VCS is the first listed.
NCT07222150 reports a single indexed study location in North Carolina.
Frequently Asked Questions
What is clinical trial NCT07222150 about?
NCT07222150 is a clinical study titled "Unity VCS: A Comparison Study Evaluating Corneal Clarity and Thickness". 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 su...
What is the current status of trial NCT07222150?
This trial is currently recruiting. It is a NA study. The enrollment target is 105 participants. The study started on 2025-10-07. Estimated completion is 2026-10.
What conditions does trial NCT07222150 study?
This clinical trial studies the following conditions: Cataract.
What interventions are being tested in trial NCT07222150?
The interventions under investigation include: Cataract surgery with Unity VCS (DEVICE), Cataract surgery with Centurion with Ozil (DEVICE).
Who is sponsoring clinical trial NCT07222150?
This trial is sponsored by Metrolina Eye Associates, P, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07222150 being conducted?
This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Cataract
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT07222150's enrollment target sits among peer trials
105 35th of 83 higher than 49 of 83 other Cataract trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Cataract trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
Evaluation of Head-Mounted Spatial Computing and Three-Dimensional (3D) Visualization in Ocular Microsurgery: A Safety and Workflow Study
RECRUITING · NA
-
Results of Patients With Glaucoma Undergoing Minimally Invasive Glaucoma Surgery in Conjunction With Cataract Surgery
RECRUITING · NA
-
Quatera 700 vs. Centurion
ACTIVE NOT RECRUITING · NA
-
Cataract Monitored Anesthesia Care (MAC) Feasibility Pilot Study
ACTIVE NOT RECRUITING · NA
-
Study to Evaluate the Safety and Effectiveness of the enVista® Beyond (EY) EDF Intraocular Lens in Subjects Undergoing Cataract Extraction
ACTIVE NOT RECRUITING · NA
-
Manhattan Vision Screening and Follow-Up Study (NYC-SIGHT)
ACTIVE NOT RECRUITING · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT03372317 · 105 participants
Tau PET in Imaging and Cognition: Healthy Adults From 55-90
- NCT04253964 · 105 participants · Phase 2
Pilot Study of Performance Status 2 vs. Performance Status 0-1 Non-small Cell Lung Cancer Patients Treated With Chemo/Immunotherapy
- NCT04742452 · 105 participants · NA
Comparison of Partial Rotator Cuff Repair vs. Superior Capsular Reconstruction for Irreparable Rotator Cuff Tears
- NCT04875429 · 105 participants · NA
Zenith® Fenestrated+ Clinical Study
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI