Visual and Patient Reported Outcomes With Clareon TruPlus

Part of paid clinical trials in Saint Louis Park, Minnesota.

Sponsor
OVO LASIK + Lens
Study ID
NCT07648355
Status
Recruiting
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Conditions

  • Cataract

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Clareon TruPlus — DEVICE
    Clareon TruPlus

Study Details

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.

Key Dates

Start date
Jun 2, 2026
Status verified
Jun 2026
Primary completion
Jul 11, 2027
Completion
Jul 11, 2027

Study Design

Enrollment
40 participants (estimated)

Arms

  • Arm: Clareon TruPlus

Primary Outcome Measure

Binocular photopic DCIVA [ Time Frame: 3 months postoperatively ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Ovo Lasik + LensSaint Louis ParkMinnesota55416
Ashley Prepeluh
[email protected]
952-204-5060
Martha F Whiting, MD (PRINCIPAL_INVESTIGATOR)
Mark C Lobanoff, MD (PRINCIPAL_INVESTIGATOR)

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