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Clinical Trials/NCT00366769
NCT00366769
Completed
Not Applicable

Evaluation of Visual Outcomes, Contrast Sensitivity, Glare, and Induction of High Order Aberrations Following LASIK Surgery Using CustomVue

Medical University of South Carolina0 sites30 target enrollmentSeptember 2005
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ConditionsMyopiaAstigmatismMyopic Astigmatism

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myopia
Sponsor
Medical University of South Carolina
Enrollment
30
Primary Endpoint
Visual acuity
Status
Completed
Last Updated
19 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
September 2005
End Date
February 2006
Last Updated
19 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

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

Outcomes

Primary Outcomes

Visual acuity

Induction of high order aberrations

Secondary Outcomes

  • Contrast sensitivity & glare
  • Patient satisfaction

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