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临床试验/CTRI/2018/09/015598
CTRI/2018/09/015598已完成未知

Intra-operative infusion of Lignocaine vs. dexmedetomidine for reducing Acute Postoperative Pain After Elective Craniotomy Surgery - a Randomized Controlled Trial

institute of neurosciences0 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
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.ASA-I and II scheduled for elective craniotomy
  • 2.Either sex
  • 3.Age group 18 to 70 years
  • 4.Preop GCS 15/15
  • 5.No neuropsychiatric illness, alcohol or drug abuse
  • 6.Co-operative and able to give informed consent in person.

排除标准

  • 1.ASA III and above
  • 2.Age less than 18 years and more than 70 years
  • 3.Preoperative GCS <15
  • 4.Allergy to study drug
  • 5.Severe respiratory, renal or hepatic disease
  • 6. Psychiatric medical history
  • 7.Severe hypotension (mean arterial pressure [MAP] <60 mmHg) or bradycardia (heart rate <40 bpm), arrhythmia, or urticaria due to lignocaine or dexmedetomidine infusion during the surgery
  • 8.Patient requiring post-op mechanical ventilation (planned/unplanned)

研究者

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