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RECRUITING
NCT07648355
Visual and Patient Reported Outcomes With Clareon TruPlus
Sponsor: OVO LASIK + Lens
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.
Official title: Visual and Patient Reported Outcomes of Clareon TruPlus IOL in Cataract Surgery Patients
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
40
Start Date
2026-06-02
Completion Date
2027-07-11
Last Updated
2026-06-15
Healthy Volunteers
No
Conditions
Interventions
DEVICE
Clareon TruPlus
Clareon TruPlus
Locations (1)
Ovo Lasik + Lens
Saint Louis Park, Minnesota, United States