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

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00366769

Enrollment

Registered

2006-08-21

Start date

2005-09-30

Completion date

2006-02-28

Last updated

2006-08-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Astigmatism, Myopia, Myopic Astigmatism

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.

Interventions

DEVICEWavefront-guided LASIK using CustomVue platform

Study design

Allocation

NON_RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

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

Design outcomes

Primary

Measure	Time frame
Induction of high order aberrations	—
Visual acuity	—

Secondary

Measure	Time frame
Contrast sensitivity & glare	—
Patient satisfaction	—

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026