跳至主要内容
临床试验/NCT04375826
NCT04375826进行中(未招募)不适用

Continuous Preperitoneal Analgesia Versus Thoracic Epidural Analgesia After Open Pancreaticoduodenectomy: a Randomized Controlled Open-labeled Noninferiority Trial

Seoul National University Hospital2 个研究点 分布在 1 个国家目标入组 146 人开始时间: 2020年11月13日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
146
试验地点
2
主要终点
Mean numerical rating score for pain after operation

研究概览

简要总结

This is a prospective randomized open-label noninferiority trial that compares thoracic epidural analgesia and continuous preperitoneal analgesia after open pancreaticoduodenectomy.

详细描述

In the Enhanced recovery after surgery (ERAS) program of pancreaticoduodenectomy (PD), thoracic epidural analgesia (or epidural analgesia) was considered to be a key analgesic method because it not only effectively controls pain, but also lowers insulin resistance and helps restore bowel movement. However, epidural analgesia can cause a number of side effects despite of effective pain control. Epidural analgesia reduces peripheral vascular resistance by blocking sympathetic nerves with local anesthetics and may cause hypotension and decreasing heart rate. In addition, it can cause orthostatic hypotension, which can interfere with early ambulation after operation. In rare cases, there are potential complications of epidural abscess, meningitis, and epidural hematoma.

Continuous peritoneal analgesia using local anesthetics has recently been used as an alternative analgesic to epidural analgesia in open abdomen surgery. This is easier to perform than epidural analgesia and is known to have fewer side effects. Recently, a non-inferiority comparison study have revealed that peritoneal analgesic was not inferior to epidural analgesia in terms of pain control. However, this study included a variety of operations other than PD, and most of the incisions were substernal, not midline. In addition, the method for mounting the epidural catheter was not described. The failure rate of the epidural catheter was reported to be 15%.

The investigators will examine the effect of continuous peritoneal analgesic postoperative pain control in patients undergoing open PD to improve postoperative pain management and to create an our own ERAS program. To this end, The investigators will test non-inferiority between epidural analgesia and peritoneal analgesia.

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
Single (Participant)

入排标准

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

入选标准

  • 18 years and older
  • Disease of periampullary lesions
  • Elective open pancreaticoduodenectomy (PD): PD or pylorus preserving pancreaticoduodenectomy (PPPD)
  • Midline incision
  • Written informed consent : ability to understand and the willingness to sign a written informed consent
  • Performance status (ECOG scale): 0-1 at the time of enrollment
  • Physical status (ASA) : 1-2 grade

排除标准

  • History of any abdominal surgery (except laparoscopic appendectomy, laparoscopic/robotic cholecystectomy, laparoscopic/robotic obstetrics and gynecology surgeries,Cesarean section, laparoscopic/robotic prostate surgery)
  • Emergency operation
  • History of chronic pain
  • Chronic use of opioid, analgesics, anti-depressant, anti-epileptics (>1year)
  • Alcoholics
  • Impossible to control PCA d/t delirium, cognitive impairment
  • Contraindication for epidural analgesia
  • Patients with coagulopathy (INR>1.5, Prothrombin time>1.5, platelets <80x10^9perL) or anti-coagulants
  • Hypersensitive to fentanyl and ropivacaine
  • Need other organ resection (ex. Liver, colon)
  • Intubation

结局指标

主要结局

Mean numerical rating score for pain after operation

时间窗: 1-3 days after operation

The scale of the numerical rating score for pain is 0\~10 and higher score is worse outcome. Mean NRS pain scores are compared between two groups.

次要结局

  • Pain related factors(postoperative day 1,2,and 3)
  • QoR-15 Survey(postoperative day 1,2,and 3)
  • Recovery related factors(Within 1 week after operation)
  • Postoperative complication factors(Within 1 week after operation)
  • analgesic related factors(postoperative day 1,2,and 3)
  • Opioid related factors(postoperative day 1,2,and 3)
  • Hospital stay(at discharge)

研究者

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

Jin-Young Jang

Associate professor

Seoul National University Hospital

研究点 (2)

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