Trials / Completed
CompletedNCT01693939
Evaluation of the Post-LASIK Flap Thickness of the FS200 Femtosecond Laser Flap
A Single Center Prospective Evaluation of the Post-LASIK Flap Thickness of the FS200 Femtosecond Laser Flap
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- Durrie Vision · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to document the programmed flap thickness to achieved flap thickness using the FS200 femtosecond laser in performing LASIK procedure. The FS200 Femtosecond laser is a precision surgical device that is used to create a flap in a FDA approved LASIK procedure.
Detailed description
The objective of this study is to evaluate the thickness of the corneal flap created with the FS 200 Femtosecond laser flap during the LASIK procedure using the Visante and OptiVue OCT ultrasound devices.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | FS200 Femtosecond Laser |
Timeline
- Start date
- 2012-02-01
- Primary completion
- 2012-04-01
- Completion
- 2012-04-01
- First posted
- 2012-09-26
- Last updated
- 2013-01-25
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01693939. Inclusion in this directory is not an endorsement.