跳至主要内容
临床试验/NCT03638401
NCT03638401已完成不适用

Epidural vs. Wound Catheter Following Liver Resection

The Leeds Teaching Hospitals NHS Trust2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2014年3月3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
发起方
入组人数
80
试验地点
2
主要终点
The length of hospital stay following open liver resection

研究概览

简要总结

Good postoperative pain control after any major surgery allows early mobilization, minimises postoperative complications and reduces patient distress. Multiple different methods of delivering analgesia have been described.

This study aims to compare postoperative pain control between patients with epidural analgesia versus the combination of continuous infiltration of local anaesthetic with wound catheters, TAP block and IV PCA with opiate analgesia following open liver resection. The investigators expect that pain control will be similar between the two groups but that the utilization of wound catheters will confer benefit due to the lack of systemic side effects associated with epidural analgesia

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Other

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All adult patients scheduled to undergo an open liver resection at this hospital will be eligible to participate.

排除标准

  • Patients with a contraindication to either epidural or wound catheter
  • Inability to give written, informed consent
  • Aged less than 18 years old
  • Liver resection combined with a secondary surgical procedure
  • Body mass index of <18 or >40
  • Pregnancy or lactation
  • A history of chronic pain requiring regular opioid analgesia
  • Prisoners

研究组 & 干预措施

Standard treatment

No Intervention

Intervention arm

Active Comparator

干预措施: This arm will received perioperative transversus abdominis plane (TAP) block followed by continuous infusion of local anaestheic by wound catheters and an IV morphine PCA. (Procedure)

结局指标

主要结局

The length of hospital stay following open liver resection

时间窗: 6 months (or length of the study)

次要结局

未报告次要终点

研究者

发起方
The Leeds Teaching Hospitals NHS Trust
申办方类型
Other
责任方
Sponsor

研究点 (2)

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