Evaluation of Outcomes Following LASIK Surgery Using CustomVue

This study has been completed.
Sponsor:
Information provided by:
Medical University of South Carolina
ClinicalTrials.gov Identifier:
NCT00366769
First received: August 17, 2006
Last updated: NA
Last verified: March 2006
History: No changes posted

August 17, 2006
August 17, 2006
September 2005
Not Provided
  • Visual acuity
  • Induction of high order aberrations
Same as current
No Changes Posted
  • Contrast sensitivity & glare
  • Patient satisfaction
Same as current
Not Provided
Not Provided
 
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.

Not Provided
Interventional
Not Provided
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Myopia
  • Astigmatism
  • Myopic Astigmatism
Device: Wavefront-guided LASIK using CustomVue platform
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
30
February 2006
Not Provided

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
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
NCT00366769
MRC-05-005
Not Provided
Not Provided
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