Trials / Completed
CompletedNCT03021707
Early Feasibility Study of UV-Femtosecond Laser Assisted Lenticular Extraction
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 7 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 22 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the initial safety of the UV-FS laser in humans.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | WaveLight® Ultraviolet Femtosecond (FS) Laser System | Utilizes ultraviolet (UV) light with a wavelength of 347 nanometers (nm) for refractive error correction |
| PROCEDURE | Laser Assisted Lenticular Extraction | Used for refractive error correction |
Timeline
- Start date
- 2017-03-07
- Primary completion
- 2019-05-27
- Completion
- 2019-10-17
- First posted
- 2017-01-16
- Last updated
- 2022-04-07
Locations
4 sites across 3 countries: United States, Ireland, Singapore
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03021707. Inclusion in this directory is not an endorsement.