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Recruiting NCT07228091

NCT07228091 Surgical Procedure Efficiency Evaluation stuDy

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Clinical Trial Summary
NCT ID NCT07228091
Status Recruiting
Phase
Sponsor Alcon Research
Condition Cataract
Study Type OBSERVATIONAL
Enrollment 180 participants
Start Date 2026-02-09
Primary Completion 2026-08

Trial Parameters

Condition Cataract
Sponsor Alcon Research
Study Type OBSERVATIONAL
Phase N/A
Enrollment 180
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2026-02-09
Completion 2026-08
Interventions
UNITY VCSCONSTELLATION

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Brief Summary

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

Eligibility Criteria

Key Inclusion Criteria: * Able to understand and sign an informed consent form (ICF) that has been approved by an ethics committee. * Planned combined phacovitrectomy procedure at one of the selected surgical sites. * Planned combined phacovitrectomy procedure with 25-gauge (G) vitrectomy tools. Key Exclusion Criteria: * Unplanned/emergency phacovitrectomy. * Pregnant. * Past history of phacovitrectomy. cataract, vitrectomy in the planned operative eye. * Other protocol-defined exclusion criteria may apply.

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