Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07228091

Surgical Procedure Efficiency Evaluation stuDy

Surgical Procedure Efficiency Evaluation stuDy (SPEED): Combination Phaco-Vitrectomy Surgeries With UNITY VCS vs. Constellation in a Real-World Operating Room Setting

Status
Recruiting
Phase
Study type
Observational
Enrollment
180 (estimated)
Sponsor
Alcon Research · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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

Detailed description

Eligible subjects will undergo routine scheduled combined anterior-posterior segments surgery (phacovitrectomy). This single visit, time-and-motion study will be conducted in the United Kingdom. This study will be conducted by Alcon Vision LLC.

Conditions

Interventions

TypeNameDescription
DEVICEUNITY VCSUNITY® 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).
DEVICECONSTELLATIONCONSTELLATION 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).

Timeline

Start date
2026-02-09
Primary completion
2026-08-01
Completion
2026-08-01
First posted
2025-11-14
Last updated
2026-02-17

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT07228091. Inclusion in this directory is not an endorsement.