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临床试验/NCT03420703
NCT03420703已完成不适用

The Effect of Erector Spinae Plane Block on Postoperative Pain Following Laparoscopic Cholecystectomy: A Randomized Controlled Study

Kocaeli University2 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2018年2月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
46
试验地点
2
主要终点
24h morphine consumption

研究概览

简要总结

Erector Spinae Plane Block is a newly defined regional anesthesia technique. Its use for many indications has been identified by case reports in the literature. As the investigators have considered that erector spinae plane block could be efficacious for providing postoperative analgesia in laparoscopic cholecystectomy, the investigators have implemented application of this blockade into practice at the clinic. Main purpose of this study is to evaluate the analgesic effect of ultrasound guided erector spinae block in laparoscopic cholecystectomy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
20 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 25 - 75 years of age
  • ASA I - II
  • Undergoing elective laparoscopic cholecystectomy

排除标准

  • ASA III - IV
  • infection of the skin at the site of needle puncture area
  • patients with known allergies to any of the study drugs
  • coagulopathy
  • recent use of analgesic drugs

研究组 & 干预措施

Block group

Active Comparator

Erector espine plane block will be administrated to this group. An intravenous patient controlled analgesia device will be given to the patients postoperatively

干预措施: erector spinae plane block (Other)

Block group

Active Comparator

Erector espine plane block will be administrated to this group. An intravenous patient controlled analgesia device will be given to the patients postoperatively

干预措施: Intravenous morphine patient controlled analgesia device (Device)

control group

Sham Comparator

An intravenous patient controlled analgesia device will be given to the patients postoperatively

干预措施: Intravenous morphine patient controlled analgesia device (Device)

结局指标

主要结局

24h morphine consumption

时间窗: for postoperative 24 hour

morphine consumptions for both group will be recorded

次要结局

  • Pain(24h)
  • Postoperative nausea and vomiting(24 hour)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Can AKSU

Assistant Professor

Kocaeli University

研究点 (2)

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