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Evaluation of Outcomes Following LASIK Surgery Using CustomVue

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00366769
Recruitment Status : Completed
First Posted : August 21, 2006
Last Update Posted : August 21, 2006
Information provided by:
Medical University of South Carolina

August 17, 2006
August 21, 2006
August 21, 2006
September 2005
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  • Visual acuity
  • Induction of high order aberrations
Same as current
No Changes Posted
  • Contrast sensitivity & glare
  • Patient satisfaction
Same as current
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Evaluation of Outcomes Following LASIK Surgery Using CustomVue
Evaluation of Visual Outcomes, Contrast Sensitivity, Glare, and Induction of High Order Aberrations Following LASIK Surgery Using CustomVue
The aim of the study was to evaluate visual outcomes, contrast sensitivity, glare and induced high order aberrations induced by the new CustomVue software use for wavefront-guided LASIK.
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Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
  • Myopia
  • Astigmatism
  • Myopic Astigmatism
Device: Wavefront-guided LASIK using CustomVue platform
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
February 2006
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Inclusion Criteria:

  • Myopia 0.00 to -6.00 D
  • Astigmatism 0.00 up to -3.00 D
  • Manifest refraction spherical equivalent (MRSE) up to -6.00 D.

Exclusion Criteria:

  • History of ocular pathology
  • Previous ocular surgery
  • Large pupils (greater than 8mm diameter, infrared measurement)
  • Thin corneas (preoperatively calculated minimal residual bed < 250 um)
  • Irregular astigmatism
  • Asymmetric astigmatism
  • Unstable refraction
  • Any other condition that precludes the patient from undergoing LASIK
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
Contact information is only displayed when the study is recruiting subjects
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Medical University of South Carolina
Not Provided
Principal Investigator: Kerry D. Solomon, MD Medical University of South Carolina
Medical University of South Carolina
March 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP