Trials / Completed
CompletedNCT01061294
Evaluation of Outcomes Using the AMO Advanced Customvue™ iLasik Procedure
Evaluation of Outcomes Using the AMO Advanced Customvue™ iLasik Procedure (Wavescan Wavefront® System, Star S4 IR™ Excimer Laser System and Intralse™ FS System)
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- Sponsor
- Innovative Medical · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to assess the efficacy, predictability and safety of the Advanced CustomVue™ iLASIK procedure (WaveScan WaveFront® System, STAR S4 IR™ Excimer Laser System and IntraLase™ FS System). Patient data will be collected electronically and analyzed to determine improvements in postoperative visual acuity, visual quality and residual error.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Advanced CustomVue™ iLASIK procedure | |
| DEVICE | WaveScan WaveFront® System, STAR S4 IR™ Excimer Laser System and IntraLase™ FS System |
Timeline
- Start date
- 2009-12-01
- Primary completion
- 2010-12-01
- Completion
- 2010-12-01
- First posted
- 2010-02-03
- Last updated
- 2011-01-13
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01061294. Inclusion in this directory is not an endorsement.