CTRI/2022/01/039244尚未招募未知
â??Utilization of NIRS monitor to compare the regional cerebral oxygen saturation between dexmedetomidine and propofol sedation in mechanically ventilated critically ill patients with sepsis- A Prospective Randomized Control Trialâ??
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
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) Adult patients (greater or equal to 18 years old) on mechanical ventilation, requiring sedation and satisfying the survival sepsis guidelines criteria for the diagnosis of sepsis.
- •2)Patients expected to be on mechanical ventilation for atleast 48 hours from the time of screening for study enrollment.
排除标准
- •1)Mean arterial pressure less than 55mm Hg despite appropriate intravenous volume replacement and vasopressors.
- •2)Patients in coma or with severe cognitive deficits due to structural brain diseases such as stroke, intracranial hemorrhage, cranial trauma, malignancy, anoxic brain injury, or cerebral edema.
- •3)Benzodiazepine dependency or history of alcohol abuse based on the medical teamâ??s decision to institute a specific treatment plan involving benzodiazepines for this dependency.
- •4)Active seizures during this ICU admission being treated with intravenous benzodiazepines.
- •5)Inability to understand English/Hindi or deafness that will preclude delirium evaluation.
- •6)Documented allergy to propofol or dexmedetomidine.
- •7)Patients who are on muscle relaxant infusions at time of screening with plans to maintain paralysis greater than 48 hours.
研究者
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