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The Exploratory Clinical Trials on the Primary Safety and Effectiveness of High Myopic Posterior Scleral Fixation System

High Myopia Clinical Trial

Official title:
High Myopic Posterior Scleral Fixation System

Clinical Trial Summary

The purpose of this study is to assess the primary safety and efficacy of High Myopic Posterior Scleral Fixation System in the treatment of macular schisis caused by high myopia.

Clinical Trial Description

Posterior Scleral Reinforcement（PSR） is the only surgical method that can delay the the development of high myopia. However, The surgical method is restricted by the material source limitation and macular ischemia in the eye after reinforcement. The investigators have designed a new posterior scleral fixation system，Its basic material is medical silicone，The product is designed to solve the problem of material source limitation and macular ischemia in the eye after reinforcement. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05034016
Study type Interventional
Source GuangZhou WeiShiBo Biotechnology Co., ltd
Contact Qianying Gao, MD,Ph.D
Phone 020-28687088
Email kevin.gao@vesber.com
Status Recruiting
Phase N/A
Start date June 1, 2020
Completion date April 24, 2022
View Details
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