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临床试验/NCT05026255
NCT05026255终止不适用

Assessment of Preload Dependency Via Measurement of Peripheral Venous Pressure During an Alveolar Recruitment Manoeuvre

GCS Ramsay Santé pour l'Enseignement et la Recherche2 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2021年12月8日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
21
试验地点
2
主要终点
Primary outcome measure

研究概览

简要总结

Assessment of preload dependency via measurement of peripheral venous pressure during an alveolar recruitment manoeuvre.

Prospective multicentre open-label study of mechanically ventilated intensive care patients.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • Patients aged 18 years or older, for whom the trusted person designated by the patient or, failing that, a relative has read and signed the consent form for participation in the study
  • Patient hospitalised in intensive care, under sedation and controlled mechanical ventilation
  • Equipped with a central venous line in the superior vena cava territory and an arterial catheter.
  • Whose state of health justifies vascular filling

排除标准

  • Patient under legal protection, guardianship or curatorship
  • Pregnant or breastfeeding woman
  • Patient not affiliated to the French social security system
  • Contraindication to the realization of an alveolar recruitment maneuver

结局指标

主要结局

Primary outcome measure

时间窗: through study completion, an average of 12 hours

The correlation between the pairs of values of CVP and PVP during an alveolar recruitment manoeuvre will be evaluated by Pearson's coefficient or Spearman's coefficient if the distribution of the values is not parametric. The coefficient of determination r² will be calculated by linear regression between the 2 variables. Finally, the agreement between the two measurements will be evaluated by the Bland-Altman method: the Bland-Altman graph will be provided and the 95% agreement limits will be calculated (+/- 1.96 SD, SD being the standard deviation of the difference between the measurements).

次要结局

  • Secondary outcome measure(through study completion, an average of 12 hours)

研究者

发起方
GCS Ramsay Santé pour l'Enseignement et la Recherche
申办方类型
Other
责任方
Sponsor

研究点 (2)

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