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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