Clinical Outcomes With Bilateral Implantation of Odyssey IOLs

Mann Eye Institute

Status: Completed

Conditions: Cataract

Treatments: Device: TECNIS Odyssey IOL

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT06550375

PB-24-01

Details and patient eligibility

About

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.

Enrollment: 40 patients

Sex: All

Ages: 50+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients aged 50 years and older who underwent bilateral cataract surgery with Odyssey IOL implantation.

Exclusion criteria

• Significant ocular comorbidities (e.g., macular degeneration, glaucoma).
• < 2 weeks post YAG capsulotomy.
• Best corrected distance visual acuity worse than 20/25.

Trial design

40 participants in 1 patient group

TECNIS Odyssey IOL

Treatment:

Device: TECNIS Odyssey IOL