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
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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