跳至主要内容
临床试验/NCT04381286
NCT04381286Unknown不适用

Transpulmonary Driving Pressure in ARDS COVID19 Patients / TRANSPULMONARY-COVID19

University Hospital, Montpellier1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2019年4月1日最近更新:
适应症

试验速览

阶段
不适用
入组人数
40
试验地点
1
主要终点
Duration of mechanical Ventilation

研究概览

简要总结

A majority (65-85%) of critically ill patients admitted in intensive care units with a confirmed diagnostic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) developed an acute respiratory distress syndrome (ARDS) according to BERLIN criteria. Gattinoni et al. recently described that the ARDS related to SARS-CoV-2 was not a "Typical" ARDS. Patients affected by this infection present indeed a major hypoxemia, which was surprisingly associated in early phase with a high compliance of respiratory system, more than 50 ml/cm H2O in most cases. The cornerstone of current treatment in case of ARDS is the use of "lung protective" ventilation, including limited tidal volumes (VT), low end-inspiratory plateau pressures while maintaining sufficiently-high positive end-expiratory pressures (PEEP). However, high levels of PEEP in patients may have detrimental effects on hemodynamic status and fluid retention, particularly when the respiratory system compliance is normal. High PEEP may also lead to overdistension and an increase of alveolar dead space. The airway pressures commonly monitored does not reliably reflect the impact of pressures on the lung parenchyma. Elastance of chest wall may indeed largely influence values of airways pressions. In contrast, transpulmonary pressure obtained using esophageal pressure (Pes) directly reflect lung overdistension risk and lung properties. In order to better understand this new kind of ARDS characterized by modest recruitable profile and to better personalize mechanical ventilation setting and therapy it is obvious to precise transpulmonary pressure.

研究设计

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

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Duration of mechanical Ventilation

时间窗: 1 day

Duration of mechanical Ventilation

次要结局

  • Number of Participants with during of Acute respiratory distress syndrom (SDRA)(1 day)
  • Length of stay in intensive care unit(1 day)
  • Mortality(1 day)
  • number of patients with pulmonary complications(1 day)
  • Number of Participants with pulmonary stress and strain(1 day)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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