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Surgical Procedure Efficiency Evaluation stuDy

NCT07228091 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 180

Last updated 2026-02-17

No results posted yet for this study

Summary

The purpose of this real-world evidence study is to compare surgical procedure times for UNITY® VCS and CONSTELLATION® Vision System.

Conditions

  • Cataract
  • Vitreous Hemorrhage
  • Retinal Detachment
  • Macular Pucker
  • Macular Holes

Interventions

DEVICE

UNITY VCS

UNITY® VCS is a CE-marked, FDA-approved ophthalmic microsurgical system that is indicated for both anterior segment (i.e., phacoemulsification and removal of cataracts) and posterior segment (i.e., vitreoretinal) ophthalmic surgery. The focus of this study will be on combined anterior-posterior segments surgery (phacovitrectomy).

DEVICE

CONSTELLATION

CONSTELLATION is a CE-marked, FDA-approved ophthalmic microsurgical system that is indicated for both anterior segment (i.e., phacoemulsification and removal of cataracts) and posterior segment (i.e., vitreoretinal) ophthalmic surgery. The focus of this study will be on combined anterior-posterior segments surgery (phacovitrectomy).

Sponsors & Collaborators

  • Manchester Royal Eye Hospital

    collaborator OTHER

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Manager, Health Economics/Outcomes Research · Alcon Research, LLC

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-02-09
Primary Completion
2026-08-31
Completion
2026-08-31

Countries

  • United Kingdom

Study Locations

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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 NCT07228091 on ClinicalTrials.gov