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Clinical Trials/NCT06860061
NCT06860061Not yet recruitingNot Applicable

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

Sohag University0 sites60 target enrollmentStarted: March 1, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
60
Primary Endpoint
Changes of corneal higher-order aberrations

Study Overview

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).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Screening
Masking
None

Eligibility Criteria

Ages
18 Weeks to 45 Weeks (Child)
Sex
All
Accepts 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.

Arms & Interventions

group 1

Active Comparator

Conventional Lasik

Intervention: Laser refractive surgery (Procedure)

group 2

Active Comparator

Femto LASIK

Intervention: Laser refractive surgery (Procedure)

group 3

Active Comparator

PRK

Intervention: Laser refractive surgery (Procedure)

Outcomes

Primary Outcomes

Changes of corneal higher-order aberrations

Time Frame: 1 year

Corneal aberrometry will be performed using Sirius's Scheimpflug-Placido topography (CSO, Florence, Italy).

Changes of total ocular higher-order aberrations

Time Frame: 1 year

Wavefront refraction will be acquired by the iDesign aberrometer (Hartmann-Shack Aberrometer)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ahmed Abdeen Refai

Master degree ophthalmology department faculty of medicine Sohag University

Sohag University

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