ACTRN12616001391460尚未招募4 期
Randomized trial of pre-operative Microdacyn versus standard care for prevention of intra-operative wound contamination and post-operative infection in clean surgical procedures
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 入组人数
- 150
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
- 16 Years 至 o limit（—）
- 性别
- All
入选标准
- •Able to provide informed consent; willingness to take part.
- •To undergo a clean elective surgical procedure (e.g. joint prosthesis, arthroscopy, tendon repair, internal fixation, laminectomy, spinal fusion, pacemaker insertion, thyroid, breast surgery)
排除标准
- •Pregnancy or breastfeeding.
- •Past adverse reaction to Microdacyn, a cephalosporin antibiotic or chlorhexidine.
- •Unable to receive cefazolin as pre-operative intravenous prophylaxis (e.g. previous severe adverse reaction to a penicillin antibiotic).
- •Suspected current or previous infection on the overlying skin or in the deep tissues at the operation site.
- •At least one dose of a systemic antibiotic in the 4 days before the start of the trial (other than routine pre-operative prophylaxis).
- •The operation site is covered by plaster of Paris or a dressing during the 3 days before the operation.
研究者
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