ACTRN12615000021572已完成3 期
A Randomised Clinical Trial in Participants Undergoing Incisional Surgery, to Assess the Efficacy of Surgical Skin Preparation: A Three-armed Comparison of Chlorhexidine versus Povidone-iodine Preparations
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 3,301
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Prevention
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •All patients undergoing elective or semi-urgent incisional surgery requiring skin preparation, that have provided written informed consent and are aged 18 years and over.
排除标准
- •Patients will be excluded if they:
- •-Refuse or are unable to give written informed consent to participate in the study, or
- •-are under 18 years of age, or
- •-have a history of allergy to iodophors
- •-have a current infection at, or adjacent to the operative site
- •-have current evidence of generalised sepsis
- •-screen positive for MRO (Multi Resistant Organism)
- •-unable to attend routine follow-up appointments
- •-previous participation in this study
研究者
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