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临床试验/NCT04734340
NCT04734340Unknown不适用

The Study of EIT-guided Ventilation Strategy on ARDS Patients

Peking Union Medical College Hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
100
试验地点
1
主要终点
ventilation free days

研究概览

简要总结

This study is a clinical randomized controlled study.The objective of this study is to compare the prognosis of patients with ARDS between eit-v / q-oriented individualized ventilation strategy and traditional lung protection ventilation strategy, and to establish the demonstration application of eit-v / q-oriented ventilation strategy in ARDS

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 (Participant)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •According to ARDS Berlin standard, ARDS, PaO2 / FiO2 < 200mmhg, peep > 5cmh2o;
  • •According to clinical judgment, lung recruitment therapy is needed due to hypoxemia;
  • •The subjects or their families signed informed consent.
  • •Admission to ICU was less than 72 hours;
  • •The estimated duration of mechanical ventilation was more than or equal to 48 hours;
  • •Age ≥ 18 years old and ≤ 80 years old;

排除标准

  • •The patients with heart implants could not be monitored by EIT;
  • •Patients or their families refused to participate in the study;
  • •Hypernatremia

研究组 & 干预措施

EIT-guided group

Experimental

Treatment based on EIT

干预措施: EIT-guided PEEP setting (Procedure)

Control group

Placebo Comparator

Treatment based on ARDS-net Peep setting

干预措施: ARDS-net PEEP setting (Procedure)

结局指标

主要结局

ventilation free days

时间窗: 1 Day

次要结局

  • 28-day mortality(28 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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