NCT01226069已完成不适用
To Investigate the Effectiveness of Topical Glycerine Sulphate, Hirudoid Cream and Nil Application in Treating Peripheral Cannula Related Phlebitis
Tan Tock Seng Hospital1 个研究点 分布在 1 个国家目标入组 147 人开始时间: 2009年11月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 147
- 试验地点
- 1
- 主要终点
- Erythema size
研究概览
简要总结
The aim of the interventional study is to compare the different treatment modalities in reducing erythema size and rate of resolving phlebitis.
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
- None
入排标准
- 年龄范围
- 21 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients admitted to the study institution between Dec 2009 and Feb 2010 and observed to develop redness associated with peripheral infusion cannula.
排除标准
- •Thrombosis, poor skin condition, and pus seen at the previous puncture.
研究组 & 干预措施
Glycerine Magnesium Sulphate paste
Active Comparator
干预措施: Glycerine Magnesium sulphate paste (Drug)
Hirudoid cream
Active Comparator
Topical Mucopolysaccharide polysulphate
干预措施: Mucopolysaccharide polysulphate (Drug)
No application
Experimental
Patient will not receive any topical application to apply on the phlebitis site. The outcome assessor will monitor regularly at pre-determined schedule as patients in other active arms.
干预措施: No application (Other)
结局指标
主要结局
Erythema size
时间窗: 5 days
The incremental percentage change in erythema size
次要结局
- Time to resolve redness(5 days)
研究者
研究点 (1)
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