CompletedNot Applicable

Clinical Outcomes With Bilateral Implantation of Odyssey IOLs

United States40 participantsStarted 2024-09-05

Plain-language 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.

Who can participate

Age range50 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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.

What they're measuring

Visual Acuity at Distance (6m) logMAR

Timeframe: 3 months postoperative

Visual Acuity at Intermediate (66cm) logMAR

Timeframe: 3 months postoperative

Visual Acuity at Near (40cm) logMAR

Timeframe: 3 months postoperative

Visual Acuity at Near (33cm) logMAR

Timeframe: 3 months postoperative

Trial details

NCT IDNCT06550375

SponsorMann Eye Institute

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-03-26

Results submitted2026-02-25

View on ClinicalTrials.gov More Cataract trials