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NOT YET RECRUITING
NCT07610226
Post-refractive IOL Outcomes With Clareon TruPlus
Sponsor: Laser Defined Vision
View on ClinicalTrials.gov
Summary
This is a prospective, single-arm, single-center, single-surgeon study evaluating the Clareon TruPlus IOL in post-refractive cataract patients. Subjects will be assessed up to 3 months post-operatively. Clinical evaluations will include refractive outcomes, visual acuity, and administration of the PRISQ Questionnaire.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
35
Start Date
2026-06-23
Completion Date
2027-06-23
Last Updated
2026-05-27
Healthy Volunteers
No
Conditions
Interventions
DEVICE
Clareon TruPlus
Clareon TruPlus
Locations (1)
Physicians Protocol
Greensboro, North Carolina, United States