CTRI/2020/04/024437尚未招募未知
Feasibility and Safety of the AnaConDa device to deliver Isoflurane sedation to the elective postoperative mechanically ventilated patients: A prospective open label trial (INSTINCT I Trial)
Dept of Anaesthesia Critical Care and Pain Tata Memorial Hospital0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
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
入选标准
- •1.Age 50-80 years
- •2.Weight 50-120 kg
- •3.Elective post-operative patients anticipated to require sedation between 12 -24 for elective mechanical ventilation.
- •4.Hemodynamically stable patients (not requiring more than 0.3 microgram/kg/min of noradrenaline)
- •5.Patients willing to participate in the trial by giving written informed consent.
排除标准
- •1.Contraindications to use of HME filter during mechanical ventilation, these may include, but not limited to: excessive secretions or pulmonary hemorrhage likely to block the filter, indications for reducing apparatus dead space.
- •2.Head trauma and neurosurgical patients or mental obtundation due to any other reason preoperatively.
- •3.Patients with raised ICP.
- •4.Low GCS ( <9).
- •5.Pregnant or breast feeding women.
- •6.Family or personal history of malignant hyperthermia.
- •7.Patients already receiving sedation for more than >6 hours.
研究者
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