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Clinical Trial

Clinical Outcomes With Bilateral Implantation of Odyssey IOLs

NCT: NCT06550375 · COMPLETED

NCT IDNCT06550375
StatusCOMPLETED
Start Date2024-09-05
Completion2025-03-26

Brief Summary

This study is a single center, ambispective study of visual outcomes after successful bilateral cataract surgery. Subjects will be assessed at least 3 months postoperatively at a single visit. Clinical evaluations will include administration of the AIOLIS and OSDI questionnaires, as well as measurement of visual acuities at distance, intermediate, and near.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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