Evaluation of Outcomes Using the Amo Advanced CustomVue Ilasik Procedure
NCT00765960 · Status: WITHDRAWN · Type: OBSERVATIONAL
Last updated 2018-06-06
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).
Conditions
- Myopia
- Hyperopia
Sponsors & Collaborators
-
Medical University of South Carolina
lead OTHER
Principal Investigators
-
Kerry D Solomon, MD · Professor of Ophthalmology
Eligibility
- Min Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2008-09-30
- Primary Completion
- 2008-10-31
- Completion
- 2009-10-31
Countries
- United States
Study Locations
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