TCTR20230825001尚未招募4 期
The sevoflurane concentration for light sedation in critically ill patients: an experimental study
适应症
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Years 至 99 Years（—）
- 性别
- All
入选标准
- •Adult patients age more than and equal to 18 years old.
- •RASS > 1 and need sedation.
- •Patient on a mechanical ventilator for at least 12 hours in medical or surgical intensive care units
排除标准
- •Patients who have a history or family history of malignant hyperthermia.
- •Patients who have evidence of raised intracranial pressure.
- •Patients with low tidal volumes (<200 ml) and one-lung ventilation.patients who have persistent bronchopleural fistula despite chest tube drainage.
- •Patients with epidural or regional analgesia
- •Patients who receive vasopressor > 0.1 mcg/kg/min of norepinephrine-equivalent dose.
- •Patients who lack of commitment to ongoing critical care treatment.
- •Patients whose medication uses a nebulizer.
- •Patients cannot inform consent.
- •Patients with pulmonary disease who have a PF ratio<200.
- •Patients who have APACHE scores> 20.
研究者
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