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临床试验/PACTR202007664590852
PACTR202007664590852已完成未知

Intrathecal Versus Intravenous Tramadol in prevention of Post-spinal anaesthesia Shivering

Suez Canal University Hospitals0 个研究点目标入组 86 人开始时间: 2020年6月3日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
86

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

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
All

入选标准

  • oAge 19 – 60 years old
  • oAmerican society of anesthesia physiological status (ASA) I and II.
  • oAll lower limb surgeries under spinal anesthesia lasting not more than 2 hours.
  • oBoth male and female gender.

排除标准

  • oContraindication to neuro-axial block as patient refusal, infection at site of injection, bleeding disorders, neuropsychiatric disorders, sepsis, hypotension.
  • oAllergy to opioids or local anesthetics.
  • oChronic opioid use or other drugs that alter pain perception.
  • oFailure of spinal anesthesia requiring general anesthesia.
  • oPatients of BMI >35
  • oIntraoperative blood loss > 30% of blood volume.
  • oSpinal deformities.

研究者

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