Condition: Cataract · Sponsor: OVO LASIK + Lens
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.
This description comes directly from the study's public registry record.
Ashley Prepeluh · 952-204-5060 · ashley.prepeluh@ovoeye.com
Always discuss trial participation with your own doctor first.
| Ovo Lasik + Lens | Saint Louis Park, Minnesota, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07648355