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临床试验/EUCTR2015-001706-34-GR
EUCTR2015-001706-34-GR进行中(未招募)1 期

A Phase 2 Proof-of-concept Study to Evaluate the Efficacy and Safety of MEDI3902 in Mechanically Ventilated Patients for the Prevention of Nosocomial Pneumonia Caused by Pseudomonas aeruginosa. - EVADE

MedImmune, LLC0 个研究点目标入组 286 人开始时间: 2016年3月22日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
286

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

入选标准

  • Colonized with Pseudomonas aeruginosa in respiratory tract, expected to require prolonged intubation and mechanical ventilation, without any evidence of active pneumonia.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 143
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 143

排除标准

  • Pseudomonas disease at randomisation; lung injury score consistent with pneumonia; current lung disease; currently receiving anti-pseudomonas antibiotics; moribund patients.

研究者

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