ISRCTN71391952
已完成
3 期
Prospective, double-blind, randomized controlled single-centre trial: suppression of surgeons? skin flora during surgical procedures using a new antimicrobial surgical glove
Ansell Healthcare (Belgium)0 个研究点目标入组 52 人2012年5月8日
概览
- 阶段
- 3 期
- 干预措施
- 未指定
- 疾病 / 适应症
- Prevention of surgical site infection
- 发起方
- Ansell Healthcare (Belgium)
- 入组人数
- 52
- 状态
- 已完成
- 最后更新
- 7年前
概览
简要总结
- 2013 results in https://www.ncbi.nlm.nih.gov/pubmed/24116857 (added 21/01/2019)
研究者
入排标准
入选标准
- •1\. All surgeons agreeing to participate after appropriate orientation and instruction
- •2\. Surgeons with visibly healthy skin, without cuts or abrasions, and individuals who had not used medicated soap or medicated hand creams one week prior to the test run
- •1\. All patients undergoing carotid endarterectomy, aortic reconstruction for aneurysms or occlusive disease, or open surgical bypass for peripheral arterial occlusive disease, are eligible to be included into the study if no existing infection at any site is present.
- •2\. Patients must not have a re\-operation during the subsequent 30 days before the study
排除标准
- •1\. Individuals without visibly healthy skin, with cuts or abrasions, and individuals who had used medicated soap or medicated hand creams one week prior to the test run
- •2\. The use of alcohol\-based hand rubs containing no additional compounds with a sustained antimicrobial efficacy 24 hours before testing
- •1\. All patients for which all other procedures are performed than carotid endarterectomy, aortic reconstruction for aneurysms or occlusive disease, or open surgical bypass for peripheral arterial occlusive disease
- •2\. All patients with an existing infection at any site and patients having a re\-operation during the subsequent 30 days
结局指标
主要结局
未指定
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