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临床试验/NCT00573638
NCT00573638Unknown不适用

The Effects of the Xal-Ease Delivery Aid Device on Patient Compliance With Xalatan Eye Drops

Augusta University2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2005年2月最近更新:
适应症

试验速览

阶段
不适用
入组人数
50
试验地点
2
主要终点
The primary outcome measure is compliance with the medication XALATAN using and not using the Xal-Ease delivery aid for their glaucoma treatment.

研究概览

简要总结

The study hypothesis is that the Xal-Ease with increase patient compliance with XALATAN

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
40 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 40 to 80 years old
  • Diagnosis warranting treatment with Xalatan eye drops.
  • ambulatory and well functioning

排除标准

  • non-ambulatory
  • less than 40 or greater than 80 years old
  • Not using Xalatan eye drops

结局指标

主要结局

The primary outcome measure is compliance with the medication XALATAN using and not using the Xal-Ease delivery aid for their glaucoma treatment.

时间窗: six months

次要结局

  • To determine if any of the other factors mentioned in the survey affect compliance to their medical regimen(six months)
  • To see whether or not the Xal-Ease device helps patients conserve medication. ie - aids in drops not distilled in the eye.(6 months)

研究者

申办方类型
Other

研究点 (2)

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