Trials / Completed
CompletedNCT04936256
Evaluation of Binocular Visual Acuity and Refractive Stability in the Alcon Clareon Intraocular Lens
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 31 (actual)
- Sponsor
- Gainesville Eye Associates · Academic / Other
- Sex
- All
- Age
- 50 Years
- Healthy volunteers
- —
Summary
The objective is to evaluate refractive stability (spherical equivalent change ≤ 0.50D from 1-month to 3-months).
Detailed description
This study is a single-arm, evaluator masked clinical evaluation study of refractive stability, after successful bilateral cataract surgery. Subjects will be assessed pre-operatively, operatively and at 1 month and 3 months post-operatively. Clinical evaluations will include measurement of bilateral visual acuity, manifest refraction, and defocus curve.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Clareon | Clareon monofocal intraocular lens (IOL) |
Timeline
- Start date
- 2021-07-02
- Primary completion
- 2022-07-28
- Completion
- 2022-07-28
- First posted
- 2021-06-23
- Last updated
- 2024-08-07
- Results posted
- 2024-08-07
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04936256. Inclusion in this directory is not an endorsement.