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临床试验/NCT00667004
NCT00667004已完成2 期

Efficacy Study of Ecabet Ophthalmic Solution in Dry Eye Disease

Bausch & Lomb Incorporated1 个研究点 分布在 1 个国家目标入组 183 人开始时间: 2008年3月22日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
183
试验地点
1
主要终点
Mean Change From Baseline in Lacrimation Assessed by Schirmer's Test

研究概览

简要总结

Efficacy study of ecabet ophthalmic solution in dry eye disease

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed with dry eye disease

排除标准

  • Dry eye disease secondary to surgery

研究组 & 干预措施

1

Experimental

ecabet ophthalmic solution

干预措施: ecabet ophthalmic solution (Drug)

2

Placebo Comparator

Placebo comparator

干预措施: placebo (Drug)

结局指标

主要结局

Mean Change From Baseline in Lacrimation Assessed by Schirmer's Test

时间窗: 43 days

The Schirmer's test is used determine if tear glands produce enough tears to keep eyes adequately moist. Calibrated strips of a non-toxic filter paper are used. One free end is placed within the lower eyelid. At the conclusion of the test, the paper strip is removed from the lower eyelid and the amount of wetting of the paper strip is measured.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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