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临床试验/EUCTR2015-000629-35-GB
EUCTR2015-000629-35-GB进行中(未招募)1 期

(Feasibility) Open label Randomised Controlled Trial of Hyperoxic O2 Therapy vs. Normoxic O2 Therapy in Sepsis - HO2T or NO2T Trial

Plymouth Hospitals NHS Trust0 个研究点目标入组 50 人开始时间: 2015年7月13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)
入组人数
50

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

入选标准

  • Inclusion Criteria
  • Adult patients aged 18 years or above.
  • Diagnosed with presumed ‘Sepsis’
  • Arrive at Derriford Emergency Department by ambulance.
  • Provision of informed consent.
  • Willing to allow their General Practitioner and consultant, if appropriate,to be notified of participation in the study.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 100
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 100

排除标准

  • Exclusion Criteria
  • The participant may not enter the study if ANY of the following apply:
  • Female participants who are pregnant
  • Existing diagnosis of chronic obstructive pulmonary disease (COPD)
  • A primary diagnosis (or suspected diagnosis) of:
  • oan acute cerebral vascular event
  • oacute coronary syndrome
  • oacute pulmonary oedema
  • ostatus asthmaticus
  • omajor cardiac arrhythmia (as part of primary diagnosis)
  • odrug overdose
  • oinjury from burn or trauma
  • Participants who require immediate intubation and ventilation on arrival in the Emergency Department
  • Participants undergoing or have undergone cardiopulmonary resuscitation in the pre-hospital phase of their treatment.
  • Current participation in another Clinical Trial of an Investigational Medicinal Product (CTIMP).

研究者

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