Trials / Completed
CompletedNCT00413881
A Prospective Comparison of Alcon LADARVision Wavefront-guided LASIK Enhancement and Conventional LASIK Enhancement for the Correction of Residual Refractive Errors Following LASIK Procedures
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- Walter Reed Army Medical Center · Federal
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to conduct a prospective clinical trial to compare conventional and WFG LASIK for enhancements on post-LASIK patients. Differences in safety, efficacy, visual quality, and refractive stability will also be compared during this study.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | WAVEFRONT- GUIDED LASIK ENHANCEMENT | Laser treatment to correct residual refractive error left over from initial LASIK correction using wavefront guided LADARvision 4000 excimer laser system |
| PROCEDURE | CONVENTIONAL LASIK ENHANCEMENT | Laser treatment to correct residual refractive error left over from initial LASIK correction using LADARvision 4000 excimer laser system. |
Timeline
- Start date
- 2004-07-01
- Completion
- 2008-03-01
- First posted
- 2006-12-20
- Last updated
- 2010-01-14
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00413881. Inclusion in this directory is not an endorsement.