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Clinical Trial

Visual and Patient Reported Outcomes With Clareon TruPlus

NCT: NCT07648355 · RECRUITING

NCT IDNCT07648355
StatusRECRUITING
Start Date2026-06-02
Completion2027-07-11
SponsorOVO LASIK + Lens (OTHER)
First posted
Last updated

Brief Summary

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

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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