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Clinical Trial Summary

The purpose of this study is to determine the effectiveness of antiangiogenic therapy to choroidal neovascularization secondary to pathologic myopia.


Clinical Trial Description

The purpose of this study is to determine the effectiveness of antiangiogenic therapy to choroidal neovascularization secondary to pathologic myopia. This study is planned as a randomized, multicenter, open-label, comperative, interventional. Patients with myopia included in it will receive brolucizumab or aflibercept. The treatment proposed in this study is based on the world experience and scientific developments of the Filatov Institute of Eye Diseases and Tissue Therapy of the NAMS of Ukraine". Therefore, it is expected that the benefit/risk ratio in relation to the participation in this study should not be different from that described in the scientific literature and the benefits outweigh the risk. It is known that the absence of treatment in these diseases leads to an irreparable loss of central vision. Patients with a pathologic myopia with CNV (native) will be treated with antiangiogenic drugs according to the regimen pro re nata. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04976244
Study type Interventional
Source The Filatov Institute of Eye Diseases and Tissue Therapy
Contact Andrii MD Korol, PhD
Phone +380936327266
Email andrii.r.korol@gmail.com
Status Recruiting
Phase N/A
Start date April 1, 2021
Completion date April 1, 2022

See also
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