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临床试验/CTRI/2022/01/039244
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??

All India Institute of Medical Sciences0 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

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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