跳至主要内容
临床试验/NCT05406388
NCT05406388已完成不适用

Ultrasound-guided Bilateral Erector Spinalis Plane Block on Postoperative Pain Management in Liver Transplantation Donors

Medipol University2 个研究点 分布在 1 个国家目标入组 41 人开始时间: 2020年12月24日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
41
试验地点
2
主要终点
Opioid consumption

研究概览

简要总结

Living donor liver transplantation has become a common treatment option for patients with end-stage liver disease. Donor hepatectomy is associated with significant postoperative pain due to inverted L-shaped incision. Therefore adequate analgesia is important for recovery.

Erector Spinae Plane Block (ESPB) is a safe anesthesia technique used to provide postoperative analgesia. This study aimed to compare the novel ultrasound-guided ESPB technique with controls in terms of postoperative opioid consumption and postoperative pain control on donor patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

盲法说明

The patient and the anesthesiologist who performs postoperative pain evaluation will not know the group.

入排标准

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

入选标准

  • Donor patients scheduled for elective hepatectomy in liver transplantation surgery
  • Patients who are aged between 18-65

排除标准

  • Patients who do not accept the procedure
  • Skin infection at the site of Erector Spina Plan Block area
  • Coagulation disorder or using anticoagulant drugs
  • Known local anesthetics and opioid allergy
  • Severe pulmonary and/or cardiovascular problems
  • Substance addiction or known psychiatric or mental problems
  • Chronic painkiller usage
  • Pregnancy or lactation

结局指标

主要结局

Opioid consumption

时间窗: Change from baseline opioid consumption at postoperative 0, 2, 4, 6, 12, 24, 36 and 48 hours

The amount of fentanyl required by the patient and given by the device will be recorded for the first 48 hours.

次要结局

  • Visual Analog Scale(Change from baseline pain scores at postoperative 0, 2, 4, 6, 12, 24, 36 and 48 hours)

研究者

发起方
Medipol University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Tumay Uludag Yanaral

Assistant professor, MD

Medipol University

研究点 (2)

Loading locations...

相似试验