跳至主要内容
临床试验/NCT04761029
NCT04761029已完成不适用

Investigation of the Efficacy of Unilateral Rhomboid Intercostal and Subserratus Plane Block Application for Postoperative Analgesia in Laparoscopic Cholecystectomy

Bursa Yüksek İhtisas Education and Research Hospital1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2018年1月1日最近更新:
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
发起方
入组人数
50
试验地点
1
主要终点
tramadol consumption

研究概览

简要总结

Laparoscopic surgery is frequently used today for abdominal region operations. Laparoscopy has become the preferred treatment for cholecystectomy. Patients undergoing laparoscopic cholecystectomy suffer from acute postoperative pain despite the multimodal analgesic regimen. For this type of surgery, many different field blocks have been used for postoperative analgesia.

详细描述

In this study, the analgesic efficacy of Unilateral Rhomboid intercostal and subserratus block was investigated in patients who had laparoscopic cholecystectomy.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • American Society of Anesthesiology physical status I and II and who gave consent for the blocks were included in the study

排除标准

  • bleeding disorders,
  • mental incapacity,
  • known allergy to the local anesthetics,
  • body mass index ≥35 kg/m2

研究组 & 干预措施

grup R

Active Comparator

Unilateral Rhomboid intercostal and subserratus block + intravenous patient-controlled analgesia

干预措施: RIIS (Other)

grup R

Active Comparator

Unilateral Rhomboid intercostal and subserratus block + intravenous patient-controlled analgesia

干预措施: Tramadol (Drug)

Group P

Placebo Comparator

intravenous patient-controlled analgesia

干预措施: Tramadol (Drug)

结局指标

主要结局

tramadol consumption

时间窗: Postoperative 24 hours

tramadol consumption

次要结局

  • Numeric Rating Scale rest(postoperative 24 hours)
  • Numeric Rating Scale during movement(Postoperative 24 hours)
  • additional analgesic use(Postoperative 24 hours)
  • side effect profile(Postoperative 24 hours)
  • sensorial dermatomal block-level(30 minutes after the block administration and at the postoperative 2nd hour)

研究者

发起方
Bursa Yüksek İhtisas Education and Research Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Korgün Ökmen

Principal Investigator ,Assoc. PhD. M.D.

Bursa Yüksek İhtisas Education and Research Hospital

研究点 (1)

Loading locations...

相似试验