Clinical Trial

RLE Outcomes With Bilateral Implantation of Odyssey IOLs

Completed
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Summary
This study is a single center, ambispective study of visual outcomes after successful bilateral implantation of the Odyssey IOL. Subjects will be assessed at least 2 months postoperatively at a single visit. Clinical evaluations will include administration of the AIOLIS questionnaire, as well as measurement of visual acuities at distance, intermediate, and near, monocular (right eye) and binocular defocus curve, and refractive outcomes.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2025-05-13; most recent amendment 2026-02-25.
Status change: Recruiting → Completed 2026-02-25
Trial Details
NCT Number NCT06979557
Lead Sponsor Mann Eye Institute
Collaborators: Sengi
Conditions Refractive Lens Exchange
Enrollment 40 participants
Start Date 2025-07-21
Primary Completion 2026-01-01 (estimated)
Study Completion 2026-01-01 (estimated)
Updated on ClinicalTrials.gov 2026-02-27