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临床试验/CTRI/2018/02/012125
CTRI/2018/02/012125已完成3 期

Randomised double blind comparitivestudy of intravenous nalbuphine and tramadol for post-spinal anaesthesia shivering

Department of anaesthesiologyIGIMSPatna0 个研究点目标入组 90 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
90

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 of ASA physical status I &II
  • 2.Age between 18-50 yrs of age of either sex who have undergone routine general, orthopaedic, or gynaecological and obstetrical surgery under spinal anaesthesia.
  • 3.Post anaesthetic shivering occurring within 10min of admission to recovery room

排除标准

  • 1. <18 yrs of age& >50 yr of age
  • 2.Post anaesthetic shivering occurring after 10 min of admission to recovery room
  • 3.Known hyperthyroidism, cardiopulmonary or neuromuscular pathology
  • 4.Patients with contraindication for the use of Nalbuphine and Tramadol will not be included

研究者

发起方
Department of anaesthesiologyIGIMSPatna

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