Trials / Completed
CompletedNCT03856944
Evaluating Refractive and Visual Outcomes With the Alcon Toric ReSTOR +2.5 and +3.0 Models
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 29 (actual)
- Sponsor
- Gainesville Eye Associates · Academic / Other
- Sex
- All
- Age
- 30 Years
- Healthy volunteers
- Accepted
Summary
The study will evaluate visual acuity and visual function with a 'blended' ReSTOR Toric intraocular lens (IOL) implantation after cataract surgery.
Detailed description
The objective is to provide a normative standard for refractive and visual outcomes in eyes with significant corneal astigmatism undergoing cataract surgery with the Alcon Toric ReSTOR lens. Patients will be bilaterally implanted, with the Toric ReSTOR +2.5D model implanted in the dominant eye and the Toric ReSTOR +3.0D model implanted in the non-dominant eye.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | ReSTOR Toric | ReSTOR Toric bilateral IOL implantation |
Timeline
- Start date
- 2018-10-05
- Primary completion
- 2019-11-18
- Completion
- 2019-11-18
- First posted
- 2019-02-27
- Last updated
- 2021-08-06
- Results posted
- 2021-08-06
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03856944. Inclusion in this directory is not an endorsement.