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临床试验/TCTR20140220001
TCTR20140220001已完成3 期

Comparison of intravenous tramadol and ketamine for prevention of catheter-related bladder discomfort after laparoscopic surgery: A randomized, placebo-controlled, double-blind study

Chulalongkorn University0 个研究点目标入组 210 人开始时间: 2014年2月20日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
210

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 70 Years(—)
性别
All

入选标准

  • adult patients aged 18-70 years old with American Society of Anesthesiologists physical status I and II undergoing elective laparoscopic surgery at King Chulalongkorn Memorial Hospital

排除标准

  • patients requiring postoperative ICU admission and respiratory support
  • history of chronic pain or chronic analgesic usage or chemical substance abuse
  • history of overactive bladder (OAB) defined as urination frequency more than 3 times at night or 8 times during a 24-hour period
  • history of bladder outlet obstruction or benign prostatic hypertrophy
  • disturbance of the central nervous system
  • severe cardivascular or hepatic disease
  • end stage renal disease (urine output less than 500 ml/24 hour
  • morbid obesity (BMI >=35)
  • hypersensitivity to tramadol or ketamine
  • patients who are unable to communicate
  • patients with difficulty in urinary catheterization
  • duration of surgery longer than 4 hours
  • conversion to laparotomy

研究者

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