EUCTR2019-002571-33-FR进行中（未招募）1 期
Transcutaneous measurement of oxygen during transient hyperoxia - SCHOTT
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
- CHU Angers
- 入组人数
- 1
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
- •- Social security
- •- written informed consent
- •- cardiac output measurementscheduled within 2 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 40
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 60
排除标准
- •- Refusal to consent
- •- Adult patient protected under the law (guardianship)
- •- Pregnancy or breast-feeding women
- •- Patients unable to understand study procedures
- •- Subjects suffering from acute or decompensated heart or respiratory failure.
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