Post-refractive IOL Outcomes With Clareon TruPlus
NCT07610226 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 35
Last updated 2026-05-27
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.
Conditions
- Cataract
Interventions
- DEVICE
-
Clareon TruPlus
Clareon TruPlus
Sponsors & Collaborators
-
Sengi
collaborator INDUSTRY -
Laser Defined Vision
lead OTHER
Principal Investigators
-
Karl Stonecipher, MD · Physicians Protocol
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-06-23
- Primary Completion
- 2027-06-23
- Completion
- 2027-06-23
- FDA Device
- Yes
Countries
- United States
Study Locations
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