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临床试验/NL-OMON32848
NL-OMON32848尚未招募2 期

The use of helium after resuscitation: a safety and feasibility study - HERES

Academisch Medisch Centrum0 个研究点目标入组 25 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
尚未招募
入组人数
25

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

  • - Admission to the ICU after successful resuscitation after witnessed out-of-hospital cardiac arrest
  • - Post-anoxic coma on admission
  • - First registered rhythm ventricular fibrillation (VF) or ventricular tachycardia (VT)
  • - Return of spontaneous circulation within 30 minutes of arrest
  • - Ability to start study medication within 6 hours after arrest
  • - Treatment with induced mild hypothermia

排除标准

  • - No informed consent
  • - Co-morbidity with a life expectancy of <6 months prior to cardiac arrest
  • - Pregnancy
  • - Neurological disorder prior to cardiac arrest
  • - Severely disabled prior to arrest
  • - A pulmonary condition requiring ventilation with a FiO2 >50% and > 10 cm H2O PEEP at the time of inclusion.

研究者

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NL-OMON29256dr. B. Preckel, MD, MA, DEAA, Department of Anesthesiology, Academic Medical CenterUniversity of Amsterdam, Meibergdreef 9Postbus 22660 H1Z-120, 1100 DD AmsterdamThe NetherlandsPhone: +31 20 5662162, +31 20 5662533 (Secr.)Fax:+31 20 6979441, e-mail : b.preckel@amc.uva.nl55
The use of helium after resuscitation: a safety and... | 临床试验