跳至主要内容
临床试验/NCT01262729
NCT01262729终止2 期

Xenon and Therapeutical Hypothermia After Successful Cardiopulmonary Resuscitation

RWTH Aachen University1 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2011年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
5
试验地点
1
主要终点
Significant difference between treatment group and control group

研究概览

简要总结

In this clinical trial will be checked, whether 2 hour ventilation with xenon has neuroprotective effects in patients with out of hospital cardiac arrest and successful cardiopulmonary resuscitation

详细描述

Patients with out of hospital cardiac arrest and successful cardiopulmonary resuscitation will be randomized in two groups. First group (Treatment group) will be inhalated with xenon within 2 hours in addition to therapeutical hypothermia. The second group (Control group) will be treated with therapeutical hypothermia in accordance to international guidelines.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
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 with out of hospital cardiac arrest and successful cardiopulmonary resuscitation, which will be treated at Department of Internal Medicine I, University Hospital Aachen

排除标准

  • Patients younger than 18 years
  • Xenon allergy
  • Pregnancy
  • High expired oxygen requirement (>70%) in order to maintain adequate arterial oxygen saturation (SpO2>94%) at the beginning of treatment

研究组 & 干预措施

Xenon-Arm

Experimental

Patients in Xenon-Arm will be inhalated with xenon within 2 hours additionally to therapeutical hypothermia after successful cardiopulmonary resuscitation.

干预措施: therapeutical hypothermia (Procedure)

Xenon-Arm

Experimental

Patients in Xenon-Arm will be inhalated with xenon within 2 hours additionally to therapeutical hypothermia after successful cardiopulmonary resuscitation.

干预措施: Xenon Inhalation (Drug)

MTH

Active Comparator

Patients after successful cardiopulmonary resuscitation will be treated only with therapeutical hypothermia

干预措施: therapeutical hypothermia (Procedure)

结局指标

主要结局

Significant difference between treatment group and control group

时间窗: within 28 days after cardiac arrest

次要结局

  • Safety and efficacy of xenon ventilation within 2 hours after successful cardiopulmonary resuscitation(within 28 days after cardiac arrest)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验