A Prospective, Comparative Study to investigate the Clinical Efficacy of iLUX and IPL treatment in Dry Eye Patients with Meibomian gland dysfunction

Asan Medical Center0 个研究点目标入组 140 人开始时间: 待定最近更新: 2024年7月23日

试验速览

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•1) Patients who visited Asan Medical Center between IRB approval date and March 30, 2025 (3 months prior to June 30, 2025) and were diagnosed with dry eye syndrome with MGD and voluntarily agreed to participate in clinical trials.
•2) Mild to moderate dry eye syndrome with MGD is diagnosed by the following criteria.
•i. symptoms of dry eye syndrome persist for at least 3 months before registration of clinical trial
•ii. The TBUT is less than 10 seconds and meets at least one of the following three criteria
•a. Meibomian gland secretion is reduced during eyelid compression, showing turbid, toothpaste-like secretions, or viscous secretions.
•b. Two or more telangiectasia at the edge of your eyelid
•c. Two or more orifices for meibomian gland are blocked
•3) Age 19 years and older and under 85 years of any gender or race
•4) Ocular surface disease index (OSDI) score of 33 or lower (mild to moderate OSDI score)

•1) Sjogren’s disease
•2) all the orifices of the upper and lower meibomian glands are completely blocked and no secretion of meibum
•3) Subject with use of cyclosporine, steroids, or antibiotics (eye drops) within 2 weeks of the screening day.
•4) Subject with use of eye drops containing lipid within 2 weeks of the screening day.
•5) Wearing contact lenses within the six month of screening day.
•6) Ophthalmic surgery or trauma within the last 3 months of screening day.
•7) Subject planning eye surgery (including LASIK/LASEK) during the study period
•8) Pregnant women, lactating women and planning to pregnant women
•9) Allergic to fluorescein eye drops.
•10) Other things that are not suitable judged by an investigator

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