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Clinical Evaluation of Visual Performance, Spectacle Independence, and Patient Satisfaction With TECNIS PureSee Mini-Monovision and TECNIS PureSee-TECNIS Odyssey Mix-Match

StatusNot Yet Recruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗

Record History

  1. Study First Submitted
The purpose of the study is to evaluate the binocular clinical endpoints of distance, intermediate, and near vision and patient reported outcomes utilizing mini-monovision versus mix-match approaches for the correction of presbyopia with intraocular lenses.
Trial Details
NCT Number NCT07860567
Lead Sponsor Dr. Daniel H. Chang, MD
Collaborators: Johnson & Johnson Surgical Vision, Inc.
Conditions
(from sponsor)		 Presbyopia Correction, Presbyopia, Dysphotopsia, Visual Acuity
Related terms Cataract, Presbyopia
Enrollment 68 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov