ISRCTN99356681已完成不适用
A single-centre study of the clinical efficacy of Eakin cohesive paste
T G Eakin Limited (UK)0 个研究点目标入组 40 人开始时间: 2005年3月16日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Patients presenting wounds, stomas and fistulae with greater than 200 ml exudate per day.
排除标准
- •Patients will be excluded from the study under the following circumstances:
- •1. Where informed consent is withheld
- •2. Where the patient is unable to give informed consent due to legal incompetence
- •3. Where, in the physician's opinion, inclusion in the trial is not advised
- •4. Where the patient is presenting a critical wound, or is in an emergency situation
- •5. Where the patient is in the intensive care unit
- •6. Where there is an open wound in the peristomal region (for stoma patients only)
- •7. Where the patient is currently participating in another clinical trial
- •8. Where the patient has a known sensitivity to the product or any of its ingredients
- •8. Where the patient currently uses stoma paste as part of their regular pouching regime
研究者
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