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Study identifier: NCT07260695 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Odyssey Evaluation in Post LASIK Patients

Condition: Cataract  ·  Sponsor: Center For Sight

PhasePhase 4
Planned participants30
Who can joinAll sexes, 50 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Helga P Sandoval  ·  8438813937  ·  hps@cepmd.com

Always discuss trial participation with your own doctor first.

Locations (1)

Center For SightVenice, Florida, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07260695