跳至主要内容
临床试验/NCT05922826
NCT05922826招募中不适用

Clinical Empirical Research of ARDS

Chinese PLA General Hospital1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2023年6月18日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
200
试验地点
1
主要终点
Overall Survival

研究概览

简要总结

According to the ARDS Berlin definition, patients with severe concurrent invasive mechanical ventilation were selected, and clinical data and prognosis were collected. Samples such as blood and balf were collected for analysis based on changes in the condition.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who meet the Berlin definition of ARDS and require invasive mechanical ventilation. ARDS diagnostic criteria: according to the Berlin definition, Chest radiograph shows patchy shadows in the lungs; Respiratory failure cannot be completely caused by heart failure or excessive fluid infusion
  • ARDS onset ≤ 3 days when included in the study
  • Patient PaO2/FiO2 ≤ 200mmHg when included in the study

排除标准

  • Patients with intracranial hypertension, pleural fistula, pneumothorax, HIV, HBV, HCV
  • Age>85 years old or<18 years old
  • Pregnant patients
  • Severe hemodynamic instability (vasopressor increase>30% in the first 6 hours, or Norepinephrine>0.5 mg kg/min)
  • Patients unable to perform EIT ventilation and/or perfusion testing (unable to perform internal jugular vein catheterization, Hypernatremia, chest malformation, active implant device, unstable spinal injury or fracture, skin lesions opposite the EIT monitoring area)
  • Patients with abnormal esophageal anatomical structure and inability to indwelling gastric tubes
  • Disagreement for inclusion in this study

结局指标

主要结局

Overall Survival

时间窗: 28 days

次要结局

未报告次要终点

研究者

发起方
Chinese PLA General Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

wang kaifei

Chinese PLA General Hospital

Chinese PLA General Hospital

研究点 (1)

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