This is a controlled study to determine the effectiveness and safety of KL7016 in the treatment of adult patients with dry eye syndrome (DES).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
147
oral administration, 150mg 3tab, bid
oral administration, 150mg 3tab, bid
oral administration, 150mg 3tab, bid
The Catholic University of Korea, Seoul St. Mary's Hospital
Seoul, Banpo-daero, Seocho-gu, South Korea
Gangnam Severance Hospital
Seoul, Eonju-ro, Gangnam-gu, South Korea
Seoul National University Bundang Hospital
Gyeonggi-do, Gumi-ro 173 Beon-gil Bundang-gu, South Korea
Change in corneal staining score
Time frame: baseline, 12 weeks
Change in schirmer test score
Time frame: baseline, 4weeks, 8weeks, 12 weeks
Change in OSDI(Ocular Surface Disease Index)
Time frame: baseline, 4weeks, 8weeks, 12 weeks
Change in TFBUT(Tear Film Break-up Time)
Time frame: baseline, 4weeks, 8weeks, 12 weeks
Change in conjunctival staining score
Time frame: baseline, 4weeks, 8weeks, 12 weeks
Change in corneal staining score
Time frame: baseline, 4weeks, 8weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Korea University Guro Hospital
Seoul, Gurodong-ro, Guro-gu, South Korea
Samsung Medical Center
Seoul, Irwon-ro, Gangnam-gu, South Korea
Chonnam National University Hospital
Gwangju, Jebong-ro, Dong-gu, South Korea
Konkuk University Medical Center
Seoul, Neungdong-ro, Gwangjin-gu, South Korea
ASAN Medical Center
Seoul, Olympic-ro 43-gil, Songpa-gu, South Korea
Severance Hospital
Seoul, Yonsei-ro, Seodaemun-gu, South Korea