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临床试验/CTRI/2019/02/017762
CTRI/2019/02/017762已完成未知

Comparison of Sevoflurane consumption using the End-tidal control(TM) versus manual agent control in low flow anaesthesia using the GE AISYS CS2 workstation: a randomized control trial

Manipal hospitals Bangalore0 个研究点目标入组 70 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
70

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. Patients willing to participate in the study, willing to sign the informed consent.
  • 2. American society of anesthesiology physical status I, II
  • 3. General anaesthetia with endotracheal tube and positive pressure ventilation
  • 4. Elective surgeries
  • 5. Duration of anaesthetic requirement greater than 120 minutes.

排除标准

  • 1. Patient refusal.
  • 2. Expected duration of surgery less than 60 minutes.
  • 3. Emergency surgeries including full stomach and/or requiring rapid sequence or modified rapid sequence induction of general anaesthesia
  • 4. General anaesthesia requiring supra-glottic airway devices.
  • 5. Patients with previously secured endotracheal tube receiving sedative medication.
  • 6. Patients of American society of anesthesiology physical status III, IV.
  • 7. Anaesthesia for pregnant women and Cesarean delivery.

研究者

发起方
Manipal hospitals Bangalore

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