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临床试验/NCT03371602
NCT03371602已完成不适用

Study of the Combined Influence of Sepsis and Mechanical Ventilation on the Human Diaphragm

Hospices Civils de Lyon1 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2017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
入组人数
33
试验地点
1
主要终点
Assessment of atrophy of the myofibers of the human diaphragm

研究概览

简要总结

The aim of this study is to study the combined impact of mechanical ventilation and sepsis on the human diaphragm in order to establish the neutral, protective or destructive character of mechanical ventilation by studying the diameter of the fibers, activation of proteolytic systems, inhibition of protein synthesis, tissue inflammation as well as contractile function.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • •Patient at least 18 years of age, male or female requiring abdominal or thoracic surgery or multi-organ sampling;
  • •Affiliated to a social security or similar system;
  • •Not subject to legal protection;
  • •Having given consent to participate in the study (or consent from the trusted person)
  • •Control group (C): non-septic mesocolic programmed abdominal or thoracic surgery: gastrectomy, esophagectomy, pancreatectomy, hepatectomy
  • •Sepsis group (S): Abdominal or thoracic surgery in a septic context (peritonitis, mediastinitis, pleural abscess)
  • •Group Mechanical Ventilation (MV): Patient in brain death for which a multi organ sample is planned
  • •Mechanical Ventilation + Sepsis (S-MV) group: Patient under controlled mechanical ventilation to undergo abdominal or thoracic surgery in a septic context (peritonitis, mediastinitis, pleural abscess)

排除标准

  • •Pregnant woman (diagnosis of interrogation)
  • •severe and / or unbalanced chronic respiratory disease; severe malnutrition
  • •Long-term corticosteroids> 5mg / day for more than 1 month
  • •surgery by laparoscopic
  • •Control group: Sepsis, preoperative controlled mechanical ventilation and preoperative hemodynamic instability
  • •Mechanical Ventilation Group: Sepsis, duration of controlled mechanical ventilation <24 hours or> 7 days
  • •Sepsis Group: Preoperatively controlled mechanical ventilation
  • •Mechanical Ventilation - Sepsis Group: duration of controlled mechanical ventilation <24 hours or> 7 days

研究组 & 干预措施

control group

Experimental

non-septic mesocolic programmed abdominal or thoracic surgery: gastrectomy, esophagectomy, pancreatectomy, hepatectomy

干预措施: surgery (Procedure)

sepsis group

Experimental

Abdominal or thoracic surgery in a septic context (peritonitis, mediastinitis, pleural abscess)

干预措施: surgery (Procedure)

mechanical ventilation group

Experimental

Patient in brain death for whom a multi-organ sampling is planned

干预措施: multi-organ sampling (Procedure)

mechanical ventilation - sepsis group

Experimental

Patient under controlled mechanical ventilation to undergo abdominal or thoracic surgery in a septic context (peritonitis, mediastinitis, pleural abscess)

干预措施: surgery (Procedure)

结局指标

主要结局

Assessment of atrophy of the myofibers of the human diaphragm

时间窗: day 0 (day of the surgery)

Atrophy of the myofibers will be assessed by comparison of the cross sectional area of the three different types of myofibers between the sepsis-mechanical ventilation group and the sepsis group, the ventilation group and the control group

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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