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临床试验/IRCT138804222159N1
IRCT138804222159N1已完成2 期

Effect of preemptive subcutaneous infiltration of two doses of tramadol on post-operative pain of urologic surgeries, a double-blinded, randomized, placebo-controlled clinical trial.

Isfahan University of Medical Sciences0 个研究点目标入组 96 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
96

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
18 years 至 75 years(—)
性别
All

入选标准

  • age 18-75 years old, candidates for urologic surgeries with ASA score I-II
  • Exclusion criteria: history of opiate addiction, history of sensitivity to Tramadol, epilepsy or high ICP, chronic hepatic disease, chronic pain, obesity (BMI>30), taking of MAO inhibitors or SSRIs, any psychological or cognitional disorders that prevent the post operative evaluations, the lack of patient tendency to continue the trial for any reason

排除标准

  • 未提供

研究者

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