CTIS2022-501157-36-00进行中(未招募)1 期
Early Sedation with Dexmedetomidine vs. Placebo in Older Ventilated Critically Ill Patients - V1.0
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 3,100
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
- 65 至 65+(—)
- 性别
- All
入选标准
- •Age = 65 years, The treating clinicians believe that the patient will remain intubated and ventilated until the day after tomorrow (i.e. unlikely to be extubated the following day), Intubated and receiving invasive mechanical ventilation in an intensive care unit, The patient requires immediate ongoing sedative medication for comfort, safety and to facilitate the delivery of life support measures.
排除标准
- •Has been intubated (excluding time spent intubated within an operating theatre or transport) for greater than 18 hours in an intensive care unit, Receiving full time residential nursing care, Death is deemed both imminent and inevitable and either the attending physician, patient or substitute decision maker is not committed to active treatment, Underlying disease that makes survival to 90 days unlikely, Previously enrolled in the SPICE IV study, Proven or suspected acute primary brain lesion such as traumatic brain injury, haemorrhage, stroke, or hypoxic brain injury, Proven or suspected spinal cord injury or other pathology that may result in permanent or prolonged weakness, Admission as a consequence of a suspected or proven drug overdose or burns, Administration of or need for ongoing neuromuscular blockade, A mean arterial blood (MAP) pressure that is less than 50 mmHg, despite adequate resuscitation and vasopressor support at time of randomization, Heart rate less than 55 beats per minute unless the patient is being treated with a beta-blocker, or a high grade atrio-ventricular block in the absence of a functioning pacemaker, Known sensitivity to dexmedetomidine, Acute fulminant hepatic failure
研究者
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