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.
Study Type
OBSERVATIONAL
Enrollment
40
Clareon TruPlus
Ovo Lasik + Lens
Saint Louis Park, Minnesota, United States
RECRUITINGBinocular photopic DCIVA
Measured using a standardized ETDRS chart at 66cm.
Time frame: 3 months postoperatively
Binocular photopic CDVA
Measured using a standardized ETDRS chart at 4m.
Time frame: 3 months postoperatively
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