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临床试验/NCT02007330
NCT02007330已完成不适用

The Effect of Systemic Lidocaine Infusion to Postoperative Pain and Quality of Recovery After Laparoscopic Hernia Repair in Children

Yonsei University1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2013年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
66
试验地点
1
主要终点
Assessing postoperative pain

研究概览

简要总结

Systemic lidocaine administration may improve postoperative pain and recovery after laparoscopic inguinal hernia repair in pediatric patients

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, Investigator)

入排标准

年龄范围
1 Year 至 6 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Age between 1 and 6 year-old
  • ASA class 1 and 2
  • Pediatric Inguinal hernia patients who are scheduled for elective laparoscopic inguinal hernia repair

排除标准

  • Allergy to local anesthetics or contraindication to use of lidocaine
  • Current active upper respiratory infection or history of upper respiratory infection within 2 weeks
  • Severe cardiovascular disease
  • Renal failure
  • Liver failure
  • Neurologic and psychologic disease
  • Chronic treatment with analgesics
  • Previous history of laparoscopic operation
  • Parents' refusal

研究组 & 干预措施

Group L

Experimental

Intravenous lidocaine infusion group

干预措施: Systemic intravenous lidocaine infusion (Drug)

Group C

Placebo Comparator

Intravenous normal saline infusion - control group

干预措施: Normal saline infusion (Drug)

结局指标

主要结局

Assessing postoperative pain

时间窗: 24 hours after operation

Assessing FLACC(Face-Legs-Activity-Crying-Consolability) score at 4, 8, 12 and 24hours after operation

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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