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临床试验/KCT0004199
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

Korea University Ansan Hospital0 个研究点目标入组 52 人待定

概览

阶段
未知
干预措施
未指定
疾病 / 适应症
Diseases of the eye and adnexa
发起方
Korea University Ansan Hospital
入组人数
52
状态
已完成
最后更新
5年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
2020年6月22日
最后更新
5年前
研究类型
Interventional Study
性别
All

研究者

入排标准

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)

结局指标

主要结局

未指定

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