Trials / Completed
CompletedNCT06550375
Clinical Outcomes With Bilateral Implantation of Odyssey IOLs
Ambispective Analysis of Patient Reported Outcomes and Visual Acuity in Patients With Bilateral Implantation of Odyssey Intraocular Lenses
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 40 (actual)
- Sponsor
- Mann Eye Institute · Academic / Other
- Sex
- All
- Age
- 50 Years
- Healthy volunteers
- —
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | TECNIS Odyssey IOL | Implantation with the TECNIS Odyssey IOL |
Timeline
- Start date
- 2024-09-05
- Primary completion
- 2025-03-26
- Completion
- 2025-03-26
- First posted
- 2024-08-13
- Last updated
- 2026-04-08
- Results posted
- 2026-04-08
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06550375. Inclusion in this directory is not an endorsement.