Clinical Trial

Visual and Patient Reported Outcomes With Clareon TruPlus

Recruiting
View on ClinicalTrials.gov →
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.
Trial Details
NCT Number NCT07648355
Lead Sponsor OVO LASIK + Lens
Collaborators: Sengi
Conditions Cataract
Enrollment 40 participants
Start Date 2026-06-02
Primary Completion 2027-07-11 (estimated)
Study Completion 2027-07-11 (estimated)
Updated on ClinicalTrials.gov 2026-06-15