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Odyssey Evaluation in Post LASIK Patients

StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated December 3, 2025 (before its estimated August 18, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Study First Submitted
This prospective study evaluates the visual and refractive outcomes of the TECNIS Odyssey intraocular lens (IOL) implanted in patients with a history of myopic LASIK. Given the unique optical challenges of post-LASIK eyes, including altered corneal curvature and higher-order aberrations, the study aims to assess the IOL's performance in terms of distance, intermediate, and near vision, and patient satisfaction. Its design features may offer favorable outcomes in these patients.
Trial Details
NCT Number NCT07260695
Lead Sponsor Center For Sight
Collaborators: Sengi Clinical
Conditions
(from sponsor)		 Cataract
Related terms Cataract
Enrollment 30 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov