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Clinical Trials in Egypt / NCT07549815
Starting soon Not applicable

Measuring the Changes of the Intraocular Pressure After Corneal Laser Refractive Surgery Using Different Techniques

NCT07549815 · tracked via the Priya Life Science Egypt tracker
Sponsor
Tanta University
Phase
Not applicable
Started
2026-04-20
Last updated
2026-04-24

Condition(s) studied

Intraocular PressureRefractive Surgery

Investigational drug(s) / intervention(s)

Corvis machine

Corvis machine: Measuring intraocular pressure by different methods and compare the results

Study summary

To evaluate the changes that occur in the intraocular pressure after corneal refractive surgery either PRK , LASIK and femtosecond laser by using Corvis CT results and applanation tonometer

Eligibility

Sex
ALL
Min age
19 Years
Max age
35 Years
Healthy volunteers
No
Inclusion Criteria: * Age between 19 and 35 years old * Myopia range from (-2.00 to -6.00 Diopter) . Exclusion Criteria: * Kertoconus. * Corneal scarring. * Previous corneal infections. * Minimum corneal thickness at the thinnest location less than 400 µm. * History of uveitis or ocular allergy. * Pre-existing glaucoma.

Primary outcome measure(s)

  • Measuring intraocular pressure — -The data collected will be before that laser surgery and one month after surgery
    Intraocular pressure will be measured by in mmHg and by two methods : Corvis CT and applanation tonometer for each patient and will be recorded

Trial sites (1)

FacilityCityRegionStatus
Tanta Univeristy Hospital Tanta Egypt

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Other trials for the same condition

AI-Orchestrated Workflow Versus Consultant Ophthalmologist for Refractive Surgery and Keratoconus Diagnosis (AEYE Trial) Enrolling by invitation
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07549815 on ClinicalTrials.gov ↗ ← All trials in Egypt