NCT00946777已完成不适用
Barrier Function Measurement in Dry Eye Patients After Using Systane Ultra for 30 Days
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 19
- 主要终点
- Percent change from baseline of corneal fluorescein
研究概览
简要总结
The primary objective is to determine if there is a correlation between reductions in corneal staining and improvements in corneal barrier function.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients must have moderate corneal staining and exhibit a need to use artificial tears.
排除标准
- •Patients can not participate in any other ophthalmic drug or device clinical trial within 30 days of the baseline visit.
结局指标
主要结局
Percent change from baseline of corneal fluorescein
时间窗: 30 days
次要结局
- Adverse event occurence(30 Days)
研究者
相似试验
已完成
1 期
IVIG-eye Drops Treatment for Dry Eye DiseaseDry EyeNCT03992482Sandeep Jain, MD27
已完成
不适用
Staining in a Healthy, Non-Dry Eye PopulationNormal Healthy EyesNCT00643942Alcon Research120
Unknown
不适用
Corneal Thickness Changes in Patient Undergoing Dry Eye ManagmentDry Eye DiseaseNCT04970329University of Faisalabad96
终止
1 期
Brimonidine Eye Drops for Treatment of Ocular Graft-vs-Host Disease (oGVHD)Ocular Graft vs Host DiseaseDry EyeMeibomian Gland DysfunctionNCT02975557Sandeep Jain, MD15
招募中
不适用
The influence of corneal epithelium barrier function caused by wearing tinted contact lensesJPRN-UMIN000033147St.Marianna University School of Medicine20