Corvis Machine
DeviceMeasuring the intraocular pressure
NCT Number: NCT07599020
To evaluate the changes that occur in the intraocular pressure before and after corneal cross linking using Corvis CT.
Trial opening soon.
Get Notified19 year–35 year
All sexes
Interventional
Not applicable
This study will be prospective study. 50 Patients will be included who will undergo corneal cross linking from the out-patient clinic of Tanta University hospital between December 2025 and December 2026 will be included in the study .
Patient with age 19 till 35 years old will be included
Patient with 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
All patient will undergo full ophthalmological examination. including best corrected visual acuity, degree of myopia , average kertometry and intraocular pressure will be measured before and after cross linkage with three different techniques including Shiotz tonometry, appalanation tonometry and CORVIS machine
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Measuring the intraocular pressure
Time frame: Through the end of the study in approximately one year
Recording the intraocular pressure
Contact information is provided by the study sponsor or research team.
Tanta University
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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