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临床试验/EUCTR2013-004743-23-GB
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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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

研究者

发起方
Hull and East Yorkshire Hospital Trust

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