KCT0004199已完成未知
Prospective, Single Center Study on Comparison of the Clinical Efficacy and Patients Satisfaction of Cyporin N 0.05% Eye Drops in Dry Eye Patients with meibomian gland dysfunction
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 52
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 20(Year) 至 0No Limit（—）
- 性别
- All
入选标准
- •Subjects who visit Korea University Ansan Hospital during the study period and who diagnosed as dry eyes with meibomian gland dysfunction.
- •-Subjects who voluntarily agreed to participate in the study
- •-Subjects with symptoms of dry eyes with meibomian gland dysfunction at least 3 months
- •-Subjects who have tear break-up time less than 5 seconds
排除标准
- •- Under 20 years of age
- •- History of using topical cyclosporine A, steroid, and antibiotic eye drops within 4 weeks of screening.
- •- Subjects who wear contact lenses within 4 weeks of screening.
- •- Subjects with ocular inflammation other than meibomian gland dysfunction and dry eyes
- •- History of ophthalmologic surgery and ocular trauma within torce within 3 months of screening
- •- Subjects who are planning to undergo eye surgery during the study period
- •- Pregnant, lactating women and women who have a pregnancy plan within 26 weeks of screening
- •- Those who have hypersensitivity to research medicines
- •- Those who have allergic reactions to fluorescein or topical anesthetic
- •- History of systemic use of tetracycline derivatives (antihistamine, isotretinoin)
- •- Those judged by researchers to be unsuitable
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