EUCTR2004-001086-17-GB进行中（未招募）不适用
Prospective randomised clinical trial to assess the efficacy of 70% v/v isopropyl alcohol and 2% w/v chlorhexidine in 70% v/v isopyl alcohol for the disinfection of skin prior to peripheral venous catheterisation. - Microbial contamination associated with ChloraPrep®
Medi-Flex0 个研究点目标入组 900 人开始时间: 2005年6月27日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 900
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Patient and healthcare worker inclusion criteria
- •-Must be at least 18 years of age.
- •-Require a PVC as part of their clinical management.
- •-Willing and able to provide verbal consent.
- •Healthcare worker
- •-Competent to insert PVC as part of their clinical practice.
- •-Completion of the study training programme.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Patient and healthcare worker exclusion criteria
- •Any patient may withdraw from the study at their own request for any reason, or at the request of their medical team, the Clinical Research Nurse, the Principal Investigator or in the case of an adverse event. History of psychiatric problems or mental handicap, breast feeding and pregnant women, anyone less than 18 years of age, patients unable to give informed consent.
- •Healthcare worker
- •Any healthcare worker may withdraw from the study at their own request for any reason, or at the request of the Clinical Research Nurse or Principal Investigator.
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