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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