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临床试验/CTRI/2017/07/008978
CTRI/2017/07/008978已完成未知

Effect of Varying Doses of Oral Pregabalin as Preemptive Analgesic in patients undergoing Infraumbilical Laprotomy under Spinal Anesthesia

Azeezia Medical College0 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
已完成
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

  • Patients of either sex,between age 18 years-65years,ASA physical status 1-2,who are scheduled for infraumbilical laprotomy under Spinal Anesthesia and are willing and able to give informed consent will be recruited to the trial

排除标准

  • Patients with
  • 1.known drug allergy to pregabalin
  • 2.uncontrolled hypertension
  • 3.uncontrolled diabetes mellitus
  • 4.ischemic heart disease
  • 5.cerebrovascular disease
  • 6.renal and hepatic disease
  • 7.history of alcohol and drug abuse
  • 8.any general contraindications for spinal anaesthesia
  • 9.chronic pain and neurological disorders
  • 10.on NSAIDâ??s and on other analgesics
  • 11.Pregnancy and lactation

研究者

发起方
Azeezia Medical College

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