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临床试验/CTRI/2022/06/043137
CTRI/2022/06/043137尚未招募未知

Comparative study of intravenous lignocaine hydrochloride and dexamethasone sodium phosphate in reduction of propofol induced vascular pain

Health and family welfare department0 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

  • Patient aged 18 to 60 yrs, either sex
  • Patients scheduled for planned surgeries

排除标准

  • ASA III, IV and V
  • Age <18 and >60 yrs
  • Parents refusing to give consent
  • Patinets having pre-existing cardiac,neurological and respiratory
  • Local infection/inflammation at Intracath site
  • Emergency Surgeries
  • Known hypersensitivity to either of the study drug (Lignocaine or
  • Dexamethasone)
  • Patients having communication problems
  • Psychiatric illness
  • CNS or neuromuscular disorders
  • Patient taking pain killers chronically or sedatrives preoperatively
  • H/O drug abuse or alcoholic
  • Patients requires repid sequence induction
  • Allergic to drugs
  • Patients having difficult IV access and small caliber veins
  • Pregnant and lactating females

研究者

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