NCT07260695

Odyssey Evaluation in Post LASIK Patients

Study Evaluating Visual Outcomes in Post-Myopic LASIK Patients After Implantation of the Odyssey Intraocular Lens

• Status: Recruiting
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 30 (estimated)
• Sponsor: Center For Sight · Academic / Other
• Sex: All
• Age: 50 Years
• Healthy volunteers: Not accepted

Summary

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.

Conditions

• Cataract

Interventions

Type	Name	Description
DEVICE	Odyssey intraocular lens	The Odyssey intraocular lens is intended to be implanted at the time of cataract surgery to replace the natural lens.

Timeline

• Start date: 2025-08-18
• Primary completion: 2026-08-18
• Completion: 2026-08-18
• First posted: 2025-12-03
• Last updated: 2025-12-03

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study