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临床试验/NCT01600651
NCT01600651已完成4 期

Effects Of A Recruitment Maneuver On Plasma Levels of sRAGE, The Soluble Form of The Receptor For Advanced Glycation End Products, In Patients With Diffuse Acute Respiratory Distress Syndrome (ARDS)

University Hospital, Clermont-Ferrand2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2012年4月1日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
24
试验地点
2
主要终点
Plasma sRAGE

研究概览

简要总结

RAGE, the receptor for advanced glycation end products, is a novel marker of alveolar epithelial type I cell injury, and soluble RAGE (sRAGE) is elevated in the plasma and in the pulmonary edema fluid from patients with ALI/ARDS. Few data are available about the influence of ventilatory interventions on levels of sRAGE in the setting of ALI/ARDS. The purpose of this prospective monocentric randomized controlled cross-over study is to describe the effects of a recruitment maneuver (RM) on plasma sRAGE levels during diffuse ARDS.

详细描述

BACKGROUND:

The receptor for advanced glycation end products (RAGE) is now identified as a marker of alveolar type I cell injury. RAGE is a member of the immunoglobulin superfamily that acts as a multiligand receptor and is involved in propagating inflammatory responses. While the precise function of RAGE remains unclear, the elevated levels of RAGE, and its soluble isoform sRAGE, correlate with severity of ALI/ARDS in human and animal studies, and higher sRAGE levels could reflect impaired alveolar fluid clearance. Lung morphology, as assessed by loss of aeration distribution patterns on computed tomography (CT) scan, predicts the response to recruitment maneuvers in patients with ARDS: patients presenting with nonfocal (diffuse) lung morphology are more likely to respond to a RM, resulting in an increase in arterial oxygenation, net alveolar fluid clearance, and significant alveolar recruitment as revealed by pressure-volume curve analysis.

DESIGN NARRATIVE:

The purpose of this prospective, randomized and controlled, cross-over study is to compare the effects of a RM on plasma sRAGE levels (measured 5 minutes before, 5 minutes, 30 minutes, 1 hour, 4 hours and 6 hours after the RM) and plasma sRAGE levels measured during a "sham" or "control" sequence, in patients with diffuse ARDS.

Mechanically ventilated ICU patients with ARDS criteria (based on the 1994 American-European Consensus Conference definition for ARDS) and nonfocal CT scan lung morphology will be included within 24 hours of disease onset. Then, patients will be randomized into 2 groups: a "RM-SHAM" group when RM sequence precedes a sham evaluation period, and a "SHAM-RM" group, in which patients receive a sham sequence before the RM sequence. Patients will receive protective ventilation, as recommended, before, during and after evaluation periods. RM consists of the application of 40 cmH20 airway pressure for 40 seconds.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Participant)

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

  • ICU patients under mechanical ventilation
  • Patients within the first 24 hours after onset of ARDS according to the 1994 American-European Consensus Conference (AECC)
  • PaO2/FiO2 ratio < 200 with external PEEP >5 cmH2O
  • "Nonfocal" loss of aeration based on CT scan lung morphology analysis, as defined by the "CT scan ARDS study group" criteria

排除标准

  • Pregnancy
  • Acute exacerbation of diabetes
  • Dialysis for end-stage kidney disease
  • Alzheimer's disease
  • Amyloidosis
  • Evolutive neoplastic lesion
  • Known or suspected history of allergy to cisatracurium
  • Chronic respiratory disease requiring long term oxygen therapy or long term ventilation
  • Confirmed or suspected elevated intracranial pressure
  • Confirmed or suspected bronchopleural fistula, pneumothorax
  • Persistent hemodynamic instability despite appropriate resuscitation

研究组 & 干预措施

Sham Recruitment (RM) maneuver group

Sham Comparator

a group in which patients receive a sham sequence before the RM sequence

干预措施: Sham recruitment maneuver (RM) group (Other)

Recruitment maneuver (RM) sham group

Sham Comparator

when recruitment maneuver sequence precedes a sham evaluation period

结局指标

主要结局

Plasma sRAGE

时间窗: 1 hour after the RM

次要结局

  • Kinetics of sRAGE after RM(5 minutes before, and 5 minutes, 30 minutes, 1 hour, 4 hours and 6 hours after RM and after a sham period)
  • Plasma sRAGE in responders and non-responders to RM(5 minutes before, then 5 minutes, 30 minutes, 4 hours and 6 hours after RM)
  • Correlation of plasma sRAGE and response to RM with lung aeration(5 minutes before, and 5 minutes, 30 minutes, 1 hour, 4 hours and 6 hours after RM or sham period)
  • Risk of RM-related pulmonary bacterial translocation(5 minutes before and 30 minutes after RM)
  • Predictive value of baseline sRAGE on the response to RM(5 minutes before, and 5 minutes, 30 minutes, 1 hour, 4 hours and 6 hours after RM)

研究者

发起方
University Hospital, Clermont-Ferrand
申办方类型
Other
责任方
Sponsor

研究点 (2)

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