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Clinical Trial Summary

Our study aims to determine the efficacy and safety of the monofocal plate haptic intraocular lens to be implanted in patients planning for cataract surgery and to determine the complications that may develop due to the lens.


Clinical Trial Description

This study was planned to be performed on 300 eyes with surgical indication due to cataracts in Van Yüzüncü Yıl University Faculty of Medicine Ophthalmology Outpatient Clinic. Uncorrected and best-corrected visual acuity, subjective refraction, slit-light biomicroscopy, optical biometry, anterior segment optical coherence tomography, intraocular pressure, endothelial cell count in the pre-and postoperative (1st, 3rd, and 12th months) controls of the patients. Fundus examination will be performed, and postoperative complications and accompanying ocular pathologies will be recorded. Data before and after surgery effectiveness will be evaluated. Reliability will be interpreted by considering postoperative complications. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06238271
Study type Interventional
Source Yuzuncu Yil University
Contact Erbil Seven, MD, Associate Professor
Phone +90 (432) 2150474
Email erbilseven@gmail.com
Status Recruiting
Phase N/A
Start date November 23, 2022
Completion date May 2025

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