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Clinical Trial Summary

In the study, The Investigators will compare the participates' corneal biomechanical properties including: Deformation Amplitude ratio (Da Ratio) Integrated Radius (IR) Stress strain index (SSI) All measurements will be taken before and after 3 months of LVC.


Clinical Trial Description

Each Participant will undergo preoperative pentacam and corvis scan for his eyes and the 3 months post operative. The participants are divided into 3 groups, one who underwent LASIK, one PRK and one Femto LASIK. Collected data will before and after surgery will be compared in each arm and then the 3 arms will be compared together. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05377099
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase N/A
Start date January 1, 2022
Completion date January 30, 2023

See also
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