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临床试验/NCT03711331
NCT03711331已完成不适用

Impact of a Strategy Based on the Unyvero® Testing System on Appropriate and Targeted Antimicrobial Treatment in Patients With Suspected VAP or HAP Requiring Mechanical Ventilation: a Randomized Controlled Unblinded Trial

University Hospital, Lille1 个研究点 分布在 1 个国家目标入组 161 人开始时间: 2020年6月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
161
试验地点
1
主要终点
Percentage of patients with targeted antibiotics regimen 24 hours after starting antimicrobial therapy in the experimental group compared to control group

研究概览

简要总结

VAPERO is a randomized, unblinded, controlled study to measure the impact of a strategy based on the Unyvero® multiplex PCR test on the adjustment of antimicrobial therapy in patients suspected with ventilator-associated or hospital-acquired pneumonia (VAP/HAP) requiring mechanical ventilation. The gold-standard microbiological diagnostic method for pneumonia in the ICU is still culture-based identification and antimicrobial susceptibility testing (AST) despite being more than a hundred years old, with results turnaround time spanning over several days, exposing patients to potentially inappropriate broad-spectrum antimicrobial therapy. The investigators aim to measure the impact of the Unyvero® testing strategy to improve the percentage of patients with VAP or HAP receiving early targeted antimicrobial therapy compared to standard care.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Investigator)

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 hospitalized in the ICU
  • suspected with VAP or HAP requiring MV

排除标准

  • Severe immunodeficiency
  • Moribund patients (SAPS II > 90)

研究组 & 干预措施

FilmArray® Pneumonia panel plus strategy

Experimental

patients benefiting from the new strategy based on the system Unyvero ®

干预措施: FilmArray® Pneumonia panel plus (Other)

Standard care

Sham Comparator

patients benefiting from usual standard care

干预措施: Standard care (Other)

结局指标

主要结局

Percentage of patients with targeted antibiotics regimen 24 hours after starting antimicrobial therapy in the experimental group compared to control group

时间窗: 24 hours after the initiation of empiric antimicrobial therapy

次要结局

  • Percentage of patients receiving appropriate antimicrobial therapy 24 hours after antibiotics initiation(24 hours after antibiotics start Daily until 7 days after antibiotics start 14 days after antibiotics start 28 days after antibiotics start)
  • Amount of days alive and free from mechanical ventilation at day 28 after antibiotics initiation.(24 hours after antibiotics start Daily until 7 days after antibiotics start 14 days after antibiotics start 28 days after antibiotics start)
  • Number of Patient Deaths(at 28 days after antibiotics start)
  • Length of stay in Intensive Care Unit(24 hours after antibiotics start Daily until 7 days after antibiotics start 14 days after antibiotics start 28 days after antibiotics start)
  • number of patient deaths in ICU(24 hours after antibiotics start Daily until 7 days after antibiotics start 14 days after antibiotics start 28 days after antibiotics start)

研究者

发起方
University Hospital, Lille
申办方类型
Other
责任方
Sponsor

研究点 (1)

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