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Clinical Trial Summary

This study aims to evaluate the efficacy and safety of 3% Diquafosol Ophthalmic Solution for visual display terminal (VDT)-associated dry eye and to investigate the mechanism of treatment.


Clinical Trial Description

The treatment period is 12 weeks. The day after subjects who meet the inclusion criteria undergo baseline examination is the day starting the medication. The dosing frequency was six times daily for 3% Diquafosol Ophthalmic Solution. The follow-up time points are 2, 4, 8, 12 weeks, and the investigator will evaluate the symptoms and signs of Dry Eye. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04668118
Study type Interventional
Source Peking University Third Hospital
Contact Hong Qi, Phd
Phone 010-13901066889
Email doctorqihong@163.com
Status Recruiting
Phase Phase 4
Start date February 1, 2021
Completion date March 25, 2023

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