EUCTR2013-004743-23-GB进行中(未招募)1 期
A randomised controlled trial to assess the clinical and cost effectiveness of pre-operative skin cleansing with chlorhexidine and povidone-iodine in preventing surgical site infection and establish the impact of aqueous versus alcoholic solutions, in patients undergoing clean or clean-contaminated, non-implant vascular surgery. - Chlorhexidine Against Povidone-Iodine Trial (CAPIT)
Hull and East Yorkshire Hospital Trust0 个研究点开始时间: 2013年11月22日最近更新:
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相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
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
- •Inclusion Criteria
- •a. Adults =18 yrs undergoing clean/ clean-contaminated non-implant vascular surgery.
- •b. Ability to understand the Patient Information Sheet and capable and willing to give informed consent and follow the protocol requirements (including attending all
- •follow- up visits)
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 650
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 220
排除标准
- •Exclusion criteria;
- •a. Patients on antibiotics for other conditions at the time of surgery or in the follow up period.
- •b. Allergies to chlorhexidine/ alcohol/ iodophors
- •c. Inability to give informed consent
- •d. Aged under 18 years at time of recruitment
- •e. Use of investigational drug/device therapy within preceding 4 weeks that may interfere with this study
- •Withdrawal criteria;
- •a)Patient request
- •b)Patient non compliance with study protocol
- •c)Patient suffers an adverse event/ reaction such that they cannot continue
- •d)Patient dies
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