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临床试验/PACTR202103703462058
PACTR202103703462058尚未招募未知

Postoperative pain management in emergency abdominal surgery: bimodal versus unimodal analgesia

Frank Enoch Gyamfi0 个研究点目标入组 108 人开始时间: 2021年3月26日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
108

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
All

入选标准

  • Patients between 18 and 80 years of age.
  • Patients undergoing emergency abdominal surgery
  • Anticipated abdominal incision of at least 5cm long
  • Patients who consent to take part in the study

排除标准

  • Patients who are allergic to paracetamol or morphine
  • Patients with impaired hepatic function or clinical features of liver disease
  • Patients with renal impairment and CrCl < 60ml/min
  • Patients with chronic opioid dependence
  • Patients who are critically ill and may need ICU care
  • Patients with a neuropsychiatric condition that may impair pain assessment

研究者

发起方
Frank Enoch Gyamfi

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