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Clinical Trials/NCT00366769
NCT00366769CompletedNot 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 enrollmentStarted: September 2005Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Primary Endpoint
Visual acuity
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsRecords & IdentifiersSimilar Trials

Study 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.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Investigators

Sponsor Class
Other

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