跳至主要内容
临床试验/EUCTR2006-001814-34-NO
EUCTR2006-001814-34-NO进行中(未招募)1 期

Effects of hypothermia on the disposition of morphine, fentanyl, midazolam and propofol in intensive care unit patients

The Norwegian University of Science and Technology0 个研究点目标入组 30 人开始时间: 2006年7月12日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
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 clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Patients treated with therapeutic hypothermia (33-34°C) and a control group of critically ill patients at a normal temperature (36-38°C).
  • Controls will be matched on sex, age and duration of morphine infusion.
  • Patients must be 18 years or older.
  • Receiving continuous analgesia/sedation with morphine and midazolam for at least 12 hours.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Pregnant women
  • Cardiovascular unstable patients in deteriorating circulating status.
  • Renal failure calculated or measured renal clearance to less than 30.
  • Clinical significant liver failure.
  • Hemoglobin < 11 g/
  • Known history of drug abuse (including cocaine, opiates, amphetamines, etc.) and alcoholism
  • History of drug allergies for the study drugs

研究者

发起方
The Norwegian University of Science and Technology

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