Trials / Terminated
TerminatedNCT05961046
Visual Performance of the Vivity IOL in Post-myopic LASIK and PRK Patients
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 6 (actual)
- Sponsor
- Laser & Corneal Surgery Associates · Academic / Other
- Sex
- All
- Age
- 40 Years
- Healthy volunteers
- Not accepted
Summary
The objective is to evaluate visual outcomes and patient satisfaction in patients with a history of myopic LASIK or PRK who will have completed cataract surgery with the Vivity IOL.
Detailed description
This study Prospective, non-interventional, single-center, single-surgeon, single-arm observational study of visual outcomes and patient satisfaction in patients with a history of myopic LASIK or PRK who will have completed cataract surgery with the Vivity IOL. Subjects will be assessed at least 3 months postoperatively. Clinical evaluations will include administration of a satisfaction questionnaire (IOLSAT), as well as measurement of binocular and monocular visual acuities, defocus curve, and manifest refraction.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Vivity IOL | Vivity IOL |
Timeline
- Start date
- 2023-08-17
- Primary completion
- 2024-06-13
- Completion
- 2024-06-13
- First posted
- 2023-07-27
- Last updated
- 2024-06-17
Locations
2 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05961046. Inclusion in this directory is not an endorsement.