Evaluation of Outcomes Following LASIK Surgery Using CustomVue

Not Applicable

Completed

• Conditions: Myopia; Astigmatism; Myopic Astigmatism

• Registration Number: NCT00366769
• Lead Sponsor: Medical University of South Carolina

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2005-09
• Study Completion: 2006-02
• Status Verified: 2006-03
• Study First Submitted: 2006-08-17
• Study First Submitted QC: 2006-08-17
• Last Update Submitted: 2006-08-17
• Study First Posted: 2006-08-21
• Last Update Posted: 2006-08-21

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Visual acuity
Induction of high order aberrations

Secondary Outcome Measures

Name	Time	Method
Contrast sensitivity & glare
Patient satisfaction