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临床试验/NL-OMON42617
NL-OMON42617已完成不适用

the influence of remote ischemic preconditioning on inflammation during human endotoxemia, a pilot proof-of-principle study - RISPENDO

Intensive Care0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Age *18 and *35 yrs

排除标准

  • Use of any medication
  • Use of recreational drugs within 21 days prior to endotoxemia experiment day
  • Use of caffeine or alcohol within 1 day prior to endotoxemia experiment day
  • Previous participation in a trial where LPS was administered
  • Surgery or trauma with significant blood loss or blood donation within 3 months prior to endotoxemia experiment day
  • Participation in another clinical trial within 3 months prior to endotoxemia experiment day
  • History, signs, or symptoms of cardiovascular disease
  • History of frequent vaso-vagal collapse or of orthostatic hypotension
  • History of atrial or ventricular arrhythmia
  • Hypertension (RR systolic>160 or RR diastolic>90)
  • Hypotension (RR systolic<100 or RR diastolic<50)
  • Conduction abnormalities on the ECG consisting of a 1st degree atrioventricular block or a complex bundle branch block
  • Renal impairment: plasma creatinine>120 µmol/L
  • Liver function abnormality: alkaline phosphatase>230 U/L and/or ALT>90 U/L
  • History of asthma
  • Obvious disease associated with immune deficiency
  • CRP > 20 mg/L
  • WBC> 12x109/L or clinically significant acute illness, including infections, within 4 weeks before endotoxemia day

研究者

发起方
Intensive Care

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