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COMPLETED
NCT06550375

Clinical Outcomes With Bilateral Implantation of Odyssey IOLs

Sponsor: Mann Eye Institute

View on ClinicalTrials.gov

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 title: Ambispective Analysis of Patient Reported Outcomes and Visual Acuity in Patients With Bilateral Implantation of Odyssey Intraocular Lenses

Key Details

Gender

All

Age Range

50 Years - Any

Study Type

OBSERVATIONAL

Enrollment

40

Start Date

2024-09-05

Completion Date

2025-03-26

Last Updated

2026-04-08

Healthy Volunteers

Not specified

Conditions

Interventions

DEVICE

TECNIS Odyssey IOL

Implantation with the TECNIS Odyssey IOL

Locations (1)

Mann Eye Institute

Houston, Texas, United States