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Changes of Higher-Order Aberrations After Different Types of LASIK in Myopia

Changes of Corneal and Total Ocular Higher-Order Aberrations After Conventional LASIK, Femto-LASIK and PRK in Low and Moderate Myopia

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06860061
Enrollment
60
Registered
2025-03-05
Start date
2025-03-31
Completion date
2026-02-28
Last updated
2025-03-05

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

Conditions

Conventional LASIK, Femto-LASIK and PRK in Low and Moderate Myopia

Brief summary

This prospective comparative interventional study will enroll patients with low and moderate myopia who seek laser vision correction at Sohag Center for LASIK and Corneal Surgeries, Sohag, Egypt. Eyes included will be divided into 3 groups according to the type of refractive surgery used (conventional LASIK, Femto-LASIK and PRK) and each group will be subdivided into 2 groups according to the degree of myopia (low and moderate).

Interventions

This prospective comparative interventional study will enroll patients with low and moderate myopia who seek laser vision correction at Sohag Center for LASIK and Corneal Surgeries, Sohag, Egypt. Eyes included will be divided into 3 groups according to the type of refractive surgery used (conventional LASIK, Femto-LASIK and PRK) and each group will be subdivided into 2 groups according to the degree of myopia (low and moderate). All patients will be subjected to routine comprehensive preoperative examinations including manifest uncorrected distant visual acuity (UCDVA), best corrected distant visual acuity (BCDVA), slit-lamp examination, intraocular pressure, and fundus examination. Corneal topography and corneal aberrometry will be performed on all patients using Sirius's Scheimpflug-Placido topography (CSO, Florence, Italy). The CSO topography system analyzes a total of 6144 corneal points of a corneal area within a circular annulus outlined by an inner radius of 0.33 mm and an outer

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
NONE

Intervention model description

This prospective comparative interventional study will enroll patients with low and moderate myopia who seek laser vision correction at Sohag Center for LASIK and Corneal Surgeries, Sohag, Egypt. Eyes included will be divided into 3 groups according to the type of refractive surgery used (conventional LASIK, Femto-LASIK and PRK) and each group will be subdivided into 2 groups according to the degree of myopia (low and moderate).

Eligibility

Sex/Gender
ALL
Age
18 Weeks to 45 Weeks
Healthy volunteers
No

Inclusion criteria

Age: 18 - 45 years old. Refraction: Low and moderate grades of myopia will be included: (According to manifest refraction) low (\[0\] - ≤ \[-3\] diopters) Moderate (\[-3\] - ≤ \[-6\] diopters) With cylinder ≤ \[-1.5\] diopters.

Exclusion criteria

Any ocular surgery or medication, corneal opacities, pregnancy, lactation and keratoconus.

Design outcomes

Primary

MeasureTime frameDescription
Changes of corneal higher-order aberrations1 yearCorneal aberrometry will be performed using Sirius's Scheimpflug-Placido topography (CSO, Florence, Italy).
Changes of total ocular higher-order aberrations1 yearWavefront refraction will be acquired by the iDesign aberrometer (Hartmann-Shack Aberrometer)

Contacts

Primary Contactahmed abdeen, Master
ophthabdeen@gmail.com+201003700245

Outcome results

None listed

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