NCT07549815

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

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
8mo left

Started Apr 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress7%
Apr 2026Jan 2027

First Submitted

Initial submission to the registry

January 17, 2026

Completed
3 months until next milestone

Study Start

First participant enrolled

April 20, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

April 24, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 20, 2026

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 16, 2027

Last Updated

April 24, 2026

Status Verified

March 1, 2026

Enrollment Period

6 months

First QC Date

January 17, 2026

Last Update Submit

April 17, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Measuring intraocular pressure

    Intraocular pressure will be measured by in mmHg and by two methods : Corvis CT and applanation tonometer for each patient and will be recorded

    -The data collected will be before that laser surgery and one month after surgery

Study Arms (1)

Measuring intraocular pressure by using different techniques

EXPERIMENTAL
Other: Corvis machine

Interventions

Measuring intraocular pressure by different methods and compare the results

Measuring intraocular pressure by using different techniques

Eligibility Criteria

Age19 Years - 35 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Age between 19 and 35 years old
  • Myopia range from (-2.00 to -6.00 Diopter) .

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tanta Univeristy Hospital

Tanta, 31515, Egypt

Location

Related Publications (1)

  • 1. Bailey MD, Zadnik K (2007) Outcomes of LASIK for myopia with FDA-approved lasers. Cornea 26(3):246-254 2. Sridhar MS, Rao SK, Vajpayee RB, Aasuri MK, Hannush S, Sinha R (2002) Complications of laser-in situ-ker- atomileusis. Indian J Ophthalmol 50(4):265-282 3. Mohammadi SF, Nabovati P, Mirzajani A, Ashrafi E, Vakilian B (2015) Risk factors of regression and under- correction in photorefractive keratectomy: a case-control study. Int J Ophthalmol 18;8(5): 933-937 4. Diakonis VF, Kankariya VP, Kymionis GD, Kounis G, Kontadakis G, Gkenos E, Grentzelos MA, Hajithanasis G, Yoo SH, Pallikaris IG (2014) Long term followup of pho- torefractive keratectomy with adjuvant use of mitomycin C. J Ophthalmol 2014:821920 5- dos Santos AM, Torricelli AA, Marino GK, Garcia R, Netto MV, Bechara SJ, Wilson SE. Femtosecond Laser-Assisted LASIK Flap Complications. J Refract Surg. 2016 Jan;32(1):52-9 6- Wang LK, Tian L and Zheng YP. Determining in vivo elasticity and viscosity with dynamic Scheimpflug imaging analysis in keratoconic and healthy eyes. J Biophotonics, 2016; 9: 454-463. 7.ConsejoA,MelcerT,RozemaJJ.Introductiontomachinelearningforophthalmologists.SeminOphthalmol.2019;34(1):19 _41.

    RESULT

Central Study Contacts

Dina Tadros, Ass Professor of Ophthalmology

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Ass Professor of ophthalmology, Tanta University Hospital

Study Record Dates

First Submitted

January 17, 2026

First Posted

April 24, 2026

Study Start

April 20, 2026

Primary Completion (Estimated)

October 20, 2026

Study Completion (Estimated)

January 16, 2027

Last Updated

April 24, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will share

Results after statistical analysis will be shared in the manuscript

Locations