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To Evaluate the Efficacy and Safety of Multifocal Soft Contact Lens in Myopia Control

Myopia Clinical Trial

Official title:
A Prospective, Randomization, Double-blind Study to Evaluate the Efficacy and Safety of Multifocal Soft Contact Lens in Myopia Control

Clinical Trial Summary

The objective of this study is to investigate the efficacy and safety of soft lens in myopia control.

Clinical Trial Description

This is a prospective, randomized, paired eye comparison, double-blind study aims to evaluate the efficacy and safety of "Soft Lens" in myopia control among schoolchildren. A total of 118 eyes are planned to be enrolled and the expect duration of subject participation will be 48 weeks not including two weeks of screening period. Data such as refractive error, axial length, visual acuity, average wearing hours, self-assessment, adverse events etc. will be collected during the study. A total of 10 visits, i.e. a screening visit, a randomization visit, and 8 treatment visits are planned. Subjects will be encouraged to complete all planned visits. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03413085
Study type Interventional
Source Largan Medical Co., Ltd.
Contact
Status Completed
Phase N/A
Start date May 2, 2018
Completion date March 5, 2020
View Details
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