KCT0004516尚未招募未知
A multicenter clinical trial to evaluate the efficacy, safety and usability of cyclosporine ophthalmic nanoemulsion 0.05% compared with cyclosporine ophthalmic emulsion 0.1%
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 60
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
- 19(Year) 至 o Limit（—）
- 性别
- All
入选标准
- •1) Adult men and women over the age of 19
- •2) KCDSG guidelines diagnosed with dry eyes with moderate or higher levels
- •(1) Cornea dye score NEI = 3 points or
- •(2) TBUT =10 sec
- •3) Patients who can be monitored for at least 3 months
- •4) Those who understand this clinical trial and voluntarily agree to it in writing
排除标准
- •1) In case ophthalmic cyclosporin preparation is used by the person currently in use or within the last month
- •2) Persons with active eye infection such as Stevens-Johnson syndrome
- •3) A person with a past history of corneal transplantation or neuronutitis
- •4) Those with eye failure or condition that may affect the analysis of the research result, or those with history
- •phobiasis, conjunctival scarring caused by semisplastic cornea, sclerosis, lack of serous tear glands, conjunctivitis, corneal esophageal force, etc.
- •5) Those who are overreacting to the ingredients (cyclosporin) of the clinical trial
- •6) Pregnant or nursing mothers
研究者
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