RLE Outcomes With Bilateral Implantation of Odyssey IOLs

Completed

Conditions studied: Refractive Lens Exchange

In brief

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.

Key facts

Study ID

NCT06979557

Run by

Mann Eye Institute

People needed

40

Starts

2025-07-21

Expected to finish

2026-01-01

Last updated by the study team

2026-02-27

Who can join

Age: 40 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants will include 40 patients aged 40 years and older who have a measurable Potential Acuity Meter (PAM) of 20/20 electing to undergo bilateral refractive lensectomy surgery with IOL implantation.

You may not qualify if…

• Patients with significant ocular comorbidities (e.g., macular degeneration, glaucoma) or prior intraocular surgery will be excluded.

Where it is running

• Mann Eye Institute — Houston, Texas, United States

Full record on ClinicalTrials.gov

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