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Clinical Trial Summary

the purpose of the study is to compare the accuracy of optical and ultrasonic biometry in intraocular lens (IOL) calculation in high myopic cataractous patients


Clinical Trial Description

- Prospective interventional (QUASI experimental) comparative study - This study will be conducted on high myopic cataractous patients scheduled for phacoemulsification and IOL implantation in department of ophthalmology, Sohag university - patients will be divided into 2 groups one will be subjected to intraocular lens (IOL) calculation by optical biometry the second one will be subjected to intraocular lens (IOL) calculation by ultrasonic biometry - postoperative auto refraction after I month ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04952181
Study type Interventional
Source Sohag University
Contact Esraa A Okasha, Resident
Phone 01028909988
Email esraa011037@med.sohag.edu.eg
Status Not yet recruiting
Phase N/A
Start date July 2021
Completion date February 2022