EUCTR2020-001379-34-ES进行中(未招募)1 期
Sedation with sevoflurane versus propofol in patients with Acute Respiratory Distress Syndrome caused by COVID-19 infection
Instituto de Investigación Sanitaria INCLIVA0 个研究点目标入组 50 人开始时间: 2020年4月14日最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 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
- 性别
- All
入选标准
- •- Age 18 years or more.
- •- Diagnosis of Acute Respiratory Distress Syndrome caused by COVID19 infection.
- •- Signature of Patient's Consent or Verbal Consent of Legal Representative
- •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 10
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 40
排除标准
- •- Intracranial hypertension
- •- Hypersensitivity to the active ingredient (propofol or sevoflurane) or to any of the excipients
- •- Current volume < 250ml
- •- History of malignant hyperthermia
- •- Liver failure
- •- Neutropenia (<0.5x109)
- •- Pregnant or lactating women
- •- Have received chemotherapy in the last month since their inclusion in the study
研究者
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