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临床试验/ISRCTN02288276
ISRCTN02288276
已完成
4 期

A double-blind, randomised, single centre study to evaluate the efficacy of polyhexanide (Prontoderm®) versus placebo for topical decolonisation of methicillin-resistant Staphylococcus aureus (MRSA) carriers

Geneva University Hospitals (Hôpitaux Universitaires de Genève) (Switzerland)0 个研究点目标入组 160 人2011年3月4日

概览

阶段
4 期
干预措施
未指定
疾病 / 适应症
未指定
发起方
Geneva University Hospitals (Hôpitaux Universitaires de Genève) (Switzerland)
入组人数
160
状态
已完成
最后更新
9年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2011年3月4日
结束日期
待定
最后更新
9年前
研究类型
Interventional
性别
All

研究者

发起方
Geneva University Hospitals (Hôpitaux Universitaires de Genève) (Switzerland)

入排标准

入选标准

  • 1\. Aged greater than or equal to 18 years, either sex
  • 2\. Microbiologically documented MRSA carriage at any site, without any signs and symptoms of active MRSA infection
  • 3\. Written informed consent

排除标准

  • 1\. Active MRSA infection
  • 2\. Chronic ulcers and deep\-seated wounds colonized by MRSA
  • 3\. Presence of tracheostomy
  • 4\. Presence of external fixator colonised with MRSA
  • 5\. Unavailability of adequate help if subject is unable to self\-administer the investigational product
  • 6\. Concurrent treatment with antimicrobial agents with anti\-MRSA activity at the time of enrollment
  • 7\. Participation in another prospective clinical trial
  • 8\. Previous enrollment in the proposed study
  • 9\. Inability to understand or to follow the study protocol
  • 10\. Planned cardiac or orthopaedic implant surgery

结局指标

主要结局

未指定

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