ClinicalTrials.Veeva

Menu

Analysis of I-Trace High Order Aberrations Induced by Wavefront Optimized Ablation Profiles

A

Alexandria University

Status and phase

Completed
Phase 3
Phase 2

Conditions

Myopia

Treatments

Device: LASIK

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This work aims at the analysis of ocular aberrations induced by wave front optimized ablation profiles WFO using I-Trace aberrometer (Ray -Tracing)

Full description

The iTrace (Tracey Technologies, Houston, Tx) is uniquely designed to combine Placido corneal topography with a ray tracing aberrometer to measure quality of vision in a patient. This work aims at the analysis of ocular aberrations induced by wave front optimized ablation profiles WFO using I-Trace aberrometer (Ray -Tracing)

Enrollment

10 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Myopia up to -8.0 D and astigmatism up to -2.0D.
  2. Cases above 18 years of age with a stable refraction for at least one year.

Exclusion criteria

  1. Keratoconus.
  2. Patients with collagen diseases.
  3. Previous LASIK or any other refractive surgery.
  4. Severe dry eye syndrome.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Laser in situ keratomileusis
Experimental group
Description:
A prospective clinical study including 20 eyes of 10 cases undergoing laser in situ keratomileusis (LASIK)
Treatment:
Device: LASIK

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems