跳至主要内容
临床试验/NCT01949935
NCT01949935已完成3 期

MIR-CABG: A Randomized, Double-blind, Placebo-controlled, Single-Center Study to Evaluate the Impact of Mupirocin on Infection Rate Post Coronary Artery Bypass Grafting

Horizon Health Network1 个研究点 分布在 1 个国家目标入组 974 人开始时间: 2009年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
974
试验地点
1
主要终点
Surgical Site Infection

研究概览

简要总结

The hypothesis is that application of Mupirocin to the nose before and after coronary artery bypass grafting surgery will reduce the incidence of surgical site infections.

详细描述

Mupirocin applied to the nares is effective in eradicating nasal carriage of Staphylococcus species. Abundant evidence has documented that a majority of gram positive surgical site infections share bacterial phenotypes identical with nasal phage types. Conflicting literature exists regarding the efficacy of mupirocin in reducing the incidence of surgical site infections. A randomized prospective double-blind placebo-controlled trial is needed to help settle this question in the setting of coronary artery bypass grafting surgery where surgical site infections carry significant morbidity, cost, and mortality.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Adults >18 years old undergoing Coronary Artery Bypass Grafting Surgery (CABG) with or without concomitant cardiac valve surgery or other cardiac surgery,
  • Median sternotomy wound
  • Capable of informed consent

排除标准

  • Allergy to mupirocin or components
  • Pregnant or lactating females
  • Emergency surgery
  • Pre-existing ongoing infection

研究组 & 干预措施

Control

Placebo Comparator

Placebo made from Glaxal base Applied once 1 day preoperatively and bid for 3 days postoperatively.

干预措施: Mupirocin (Drug)

Mupirocin

Experimental

Mupirocin ointment applied to nares once 1 day preoperatively and bid for 3 days postoperatively.

干预措施: Mupirocin (Drug)

结局指标

主要结局

Surgical Site Infection

时间窗: <30 days post operation

Surgical site infections (SSI) are classified as superficial, deep, or organ surgical site infections based on CDC definition.

次要结局

  • Mortality(< or = 30 days post operation)
  • Serious adverse durg effects(< or = 30 day post operation)
  • S. aureus carrier status(< or = 30 day post operation)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr Craig Brown

Director of Clinical Trials, New Brunswick Heart Centre

Horizon Health Network

研究点 (1)

Loading locations...

相似试验