跳至主要内容
临床试验/CTRI/2015/01/005424
CTRI/2015/01/005424已完成未知

Prevention of pain due to propofol injection: A comparative study of lignocaine, dexmedetomidine and placebo.

nil0 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
未知
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

  • Written informed consent.
  • Patients of either sex.
  • Aged between 17 -70 years
  • Belonging to ASA GRADE 1 and 2( Based on the physical status,the patients are classified into categories by American Society of Anaesthesiologists)
  • Requiring standard General Anaesthesia (G.A)

排除标准

  • Concomitant analgesic or sedative medication, patients requiring rapid sequence induction, anticipated difficulty venous access, difficulty in communication
  • Known sensitivity to lignocaine or dexmedetomidine
  • Conditions where use of lignocaine and dexmedetomidine may be harmful
  • Presence of infection on the dorsum of hand

研究者

发起方
nil

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