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临床试验/NCT03560193
NCT03560193已完成4 期

An Open Label, Multicenter, Randomized Trial of 2% Chlorhexidine-70% Isopropanol vs 5% Povidone Iodine-69% Ethanol for Skin Antisepsis in Reducing Surgical-site Infection After Cardiac Surgery

Poitiers University Hospital8 个研究点 分布在 1 个国家目标入组 3,316 人开始时间: 2018年9月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
3,316
试验地点
8
主要终点
Incidence of any re-sternotomy occurring between Day 0 and Day 90 after surgery

研究概览

简要总结

Despite completion of more than 9 million procedures each year in France, the best antiseptic solution to be used for preparing the skin to reduce risk of surgical site infection (SSI) remains unknown. 2% Chlorhexidine gluconate (CHG)-alcohol is superior to Povidone Iodine (PVI)-alcohol for short term vascular catheter care (Mimoz O, Lancet 2015; Pages J, Intensive Care Med 2016), but studies comparing both antiseptic solutions for clean-contaminated surgical procedures led to conflicting results.

The present study will be the first large scale multicenter randomized controlled trial adequately powered to compare efficacy and safety of CHG-alcohol over PVI-alcohol in reducing SSI after clean surgery.

A clean surgery was chosen because pathogens involved in SSI mostly originate from skin. Therefore, optimisation of skin disinfection before surgery has the potential to reduce the incidence of SSI. Cardiac surgery was chosen because SSI may be severe, diagnosis of SSI is easy to monitor and to define and infections arise earlier than other frequent clean surgeries using implants such as orthopaedic or vascular surgery.

The incidence of reoperation for any purpose will be used as the main objective because there are easy to track and define and are less susceptible to interpretation in an open trial than superficial SSI. According to CDC criteria, patients will be monitored up to Day 90 because mediastinitis after cardiac surgery may occur after the usual 30-day SSI surveillance period.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients (age ≥ 18 years)
  • Undergoing any (scheduled) surgery of the heart (valve, coronary or combined surgery) or of the aorta via a median sternotomy
  • Having given their informed consent

排除标准

  • Patients with known allergies to CHG, PVI, isopropanol or ethanol
  • Surgery for heart transplantation
  • Any signs of inflammation or sternal instability at the site of sternotomy or operation for infection (SWI or endocarditis)
  • Patients with history of cardiac surgery within 3 months preceding enrolment
  • Participation to another clinical trial aimed at reducing SSI
  • Patients already enrolled in this study
  • Pregnant or breastfeeding women
  • Women at age to procreate and not using effective contraception
  • Patients not benefiting from a Social Security scheme or not benefiting from it through a third party
  • Persons benefiting from enhanced protection, namely minors, persons deprived of their liberty by a judicial or administrative decision, adults under legal protection.

研究组 & 干预措施

Chlorhexidine Group

Experimental

干预措施: 2%Chlorhexidine-70%Isopropanol (Drug)

Povidone Iodine Group

Active Comparator

干预措施: 5%Povidone Iodine- 69%Ethanol (Drug)

结局指标

主要结局

Incidence of any re-sternotomy occurring between Day 0 and Day 90 after surgery

时间窗: 90 days

Incidence of any reoperation on saphen venous/radial artery site occurring between Day 0 and Day 30 after surgery.

时间窗: 30 days

次要结局

  • Number of days in ICU(90 days)
  • Incidence of local and systemic side effects possibly linked to antiseptic use(90 days)
  • Incidence of superficial incisional SSIs at sternal or saphen venous/radial artery sites according to CDC criteria occurring by Day 30 after surgery and pathogens involved(30 days)
  • Economic analysis including cost-effectiveness of surgical skin antisepsis(90 days)
  • Incidence of mediastinitis according to CDC criteria occurring by Day 90 after surgery and pathogens involved(90 days)
  • Incidence of deep incisional SSIs at saphen venous/radial artery site according to CDC criteria occurring by Day 30 after surgery and pathogens involved(30 days)
  • Incidence of SWI requiring reoperation, occurring by Day 90(90 days)
  • Incidence of SSIs at saphen venous/radial artery site requiring reoperation, occurring by Day 30(30 days)
  • Mortality at Day 90 of surgery(90 days)
  • Incidence of unexpected need for re-admission to the ICU or re-hospitalisation(90 days)
  • Number of days under mechanical ventilation(90 days)
  • Number of days in Hospital(90 days)
  • Number of days in rehabilitation unit(90 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (8)

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