Evaluation of Outcomes Using the Amo Advanced CustomVue Ilasik Procedure
Withdrawn before enrolling
Conditions studied: Myopia, Hyperopia
In brief
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).
Key facts
- Study ID
- NCT00765960
- Run by
- Medical University of South Carolina
- People needed
- 0
- Starts
- 2008-09-01
- Expected to finish
- 2009-10-01
- Last updated by the study team
- 2018-06-06
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: accepted.
Where it is running
- Magill Laser Center, Medical University of South Carolina — Charleston, South Carolina, United States
Full record on ClinicalTrials.gov
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