Evaluation of Outcomes Following LASIK Surgery Using CustomVue

Medical University of South Carolina (MUSC)

Status: Completed

Conditions: Myopia; Astigmatism; Myopic Astigmatism

Treatments: Device: Wavefront-guided LASIK using CustomVue platform

Study type: Interventional

Funder types: Other

Identifiers

NCT00366769

MRC-05-005

Details and patient eligibility

About

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.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)