Odyssey Evaluation in Post LASIK Patients

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.

NCT Number	NCT07260695
Lead Sponsor	Center For Sight Collaborators: Sengi Clinical
Conditions	Cataract
Enrollment	30 participants
Start Date	2025-08-18
Primary Completion	2026-08-18 (estimated)
Study Completion	2026-08-18 (estimated)
Updated on ClinicalTrials.gov	2025-12-03