Trials / Completed
CompletedNCT01673503
A Prospective Study of Femtosecond Laser Intracorneal Lensectomi
A Prospective Study of Femtosecond Laser Intracorneal Lensectomi in Treatment of Moderate to High Myopia
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 35 (planned)
- Sponsor
- Odense University Hospital · Academic / Other
- Sex
- All
- Age
- 25 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to compare visual acuity, safety, predictability, corneal biomechanics, dry eyes, and nerve-morphology after all femtosecond laser refractive lenticule extraction. Approximately 30 to 40 patients with moderate to high myopia will randomly (after ocular dominance) receive ReLEx flex in one eye, and ReLEx smile in the other.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Carl Zeiss Meditech VisuMax laser | Refractive lenticule extraction (ReLEx) with the Carl Zeiss Meditech VisuMax laser |
Timeline
- Start date
- 2011-05-01
- First posted
- 2012-08-28
- Last updated
- 2013-01-24
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT01673503. Inclusion in this directory is not an endorsement.