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

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

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07549815
Enrollment
50
Registered
2026-04-24
Start date
2026-04-20
Completion date
2027-01-16
Last updated
2026-04-24

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

Conditions

Intraocular Pressure, Refractive Surgery

Brief 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

Detailed description

This study will be prospective study. 50 Patients who will undergo refractive surgery referred from the out-patient clinic of Tanta University hospital between December 2025 and December 2026 will be included in the study . The patient will be randomly selected to do either LASIK, PRK or femtosecond laser LASIK Patients who will undergo refractive surgery either PRK, LASIK or femtosecond laser with age between 19 and 35 years old , Myopia range from (-2.00 to -6.00 Diopter) and to maintain stability of the data we will use only the right eye of each patient will be included on the study Kertoconus, Corneal scarring, Previous corneal infections, Minimum corneal thickness at the thinnest location less than 400 µm, History of uveitis or ocular allergy and Pre-existing glaucoma will be excluded from the study. Age, sex, uncorrected distance visual acuity (UDVA), corrected distance visual acuity (CDVA), manifest and cycloplegic refraction, Slit lamp biomicroscopy, fundus examination , Central corneal thickness (CCT) and average Keratometer (K) data will be collected Intraocular pressure will be measured by by two methods : Corvis CT and applanation tonometer for each patient and will be recorded, all the data will be collected before the refractive surgery and one month after refractive surgery

Interventions

Measuring intraocular pressure by different methods and compare the results

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to 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.

Design outcomes

Primary

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

Countries

Egypt

Contacts

CONTACTDina Tadros, Ass Professor of Ophthalmology
dina.tadros@med.tanta.edu.eg+201224093354

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 25, 2026