Trials / Completed
CompletedNCT01941498
WaveLight® Refractive Myopic Study
A Prospective, Global, Multi-Center Study for the Evaluation of Outcomes on Subjects Undergoing Myopic Treatments Using the WaveLight® Refractive Suite
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 104 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate outcomes of subjects undergoing myopic surgery using the WaveLight® Refractive Suite (Excimer EX500 and Femtosecond FS200 lasers).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Wavelight® Refractive Suite | Excimer EX500 and Femtosecond FS200 lasers (Wavelight® Refractive Suite) used during LASIK surgery for corneal flap creation and corneal ablation |
| PROCEDURE | LASIK surgery | Surgical procedure for treating refractive error based on corneal reshaping |
Timeline
- Start date
- 2013-09-01
- Primary completion
- 2014-01-01
- Completion
- 2014-08-01
- First posted
- 2013-09-13
- Last updated
- 2015-11-03
- Results posted
- 2015-03-11
Source: ClinicalTrials.gov record NCT01941498. Inclusion in this directory is not an endorsement.