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临床试验/CTRI/2020/02/023522
CTRI/2020/02/023522尚未招募未知

Assessment and comparison of ketamine, dexamethasone and lignocaine in reduction of propofolâ??induced vascular pain. - nil

Department of anaesthesiology AIIMS Rishikesh0 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
发起方

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

  • The study will include patients belonging to ASA I, age group of 18 to 65 years, weighing 40-80 kg, receiving general anesthesia for elective surgery

排除标准

  • Patients with known hypersensitivity to either lignocaine or dexamethasone or ketamine or propofol or egg or soyabean oil.
  • Patients with a history of central nervous system or neuro-muscular disease or
  • psychiatric illness.
  • Patients with history of drug or alcohol abuse.
  • History of chronic pain, or taking analgesics or sedatives preoperatively.
  • Pregnant and lactating females.
  • Patients with difficult venous access and small caliber veins.
  • Patients requiring rapid sequence induction

研究者

发起方
Department of anaesthesiology AIIMS Rishikesh

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