Trials / Completed
CompletedNCT06979557
RLE Outcomes With Bilateral Implantation of Odyssey IOLs
Ambispective Analysis of Patient Reported Outcomes and Visual Acuity in Patients Undergoing a Refractive Lens Exchange With Bilateral Implantation Odyssey Intraocular Lenses
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 40 (actual)
- Sponsor
- Mann Eye Institute · Academic / Other
- Sex
- All
- Age
- 40 Years
- Healthy volunteers
- Not accepted
Summary
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Odyssey IOL | Bilateral implantation with the Odyssey IOL |
Timeline
- Start date
- 2025-07-21
- Primary completion
- 2026-01-01
- Completion
- 2026-01-01
- First posted
- 2025-05-20
- Last updated
- 2026-02-27
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06979557. Inclusion in this directory is not an endorsement.