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Clinical Trial Summary

The objective is to compare the USL and placebo in terms of efficacy and safety, and to determine the appropriate dosage.


Clinical Trial Description

This study is a phase 2, dose-finding, double-blind, randomized placebo-controlled trial of two different doses of USL compared with placebo. A total of 120 patients, aged over 19 years, with Corneal staining score(Oxford grading) ≥ 2 or TBUT < 10 sec and OSDI ≥ 10 points will be recruited at Daejeon University Daejeon Korean Medicine Hospital. Patients will take medications two times daily for 12 weeks, with 5 visiting days(screening, week 0, week 6, week 12, week 14). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06016010
Study type Interventional
Source Korea Institute of Oriental Medicine
Contact Yee Ran Lyu, PhD
Phone 82-10-9904-8049
Email onedoctor2ran@kiom.re.kr
Status Not yet recruiting
Phase Phase 2
Start date January 1, 2024
Completion date December 31, 2025

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