RecruitingNCT07610226

Post-refractive IOL Outcomes With Clareon TruPlus


Sponsor

Laser Defined Vision

Enrollment

35 participants

Start Date

Jun 23, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

This is a prospective, single-arm, single-center, single-surgeon study evaluating the Clareon TruPlus IOL in post-refractive cataract patients. Subjects will be assessed up to 3 months post-operatively. Clinical evaluations will include refractive outcomes, visual acuity, and administration of the PRISQ Questionnaire.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Clareon TruPlus for people with cataract. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEClareon TruPlus

Clareon TruPlus


Locations(1)

Physicians Protocol

Greensboro, North Carolina, United States

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NCT07610226


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