Low Concentration Atropine in the Prevention of Myopia in Children.

Status Recruiting

Clinical Trial Summary

This double-blind, randomized controlled clinical study is to evaluate the effectiveness and safety of low concentration atropine in preventing myopia in pre-myopia children, and to explore whether there is a dose effect relationship between different concentrations of atropine in preventing myopia.

Clinical Trial Description

The main questions this double-blind, randomized controlled clinical study aims to answer are: 1. To evaluate the effect of low concentration atropine on the incidence of myopia in pre myopia children. 2. To evaluate the effectiveness of low concentration atropine in controlling refractive and axial progression. Patients are randomly divided into three treatment groups with different atropine concentrations(0.01%, 0.02%, 0.04%) and one control group with atropine dissolvant. Patients are required to use the eye drops every night for one year and record after daily usage. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05939882
Study type	Interventional
Source	Shanghai Eye Disease Prevention and Treatment Center
Contact	Xiangui He
Phone	+8615000755422
Email	xianhezi@163.com
Status	Recruiting
Phase	N/A
Start date	April 1, 2023
Completion date	April 2024

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