跳至主要内容
临床试验/TCTR20211021005
TCTR20211021005Unknown4 期

Comparison of analgesic efficacy between programmed intermittent epidural bolus (PIEB) and continuous epidural infusion (CEI) of patient controlled thoracic epidural analgesia after upper abdominal surgery, a randomized controlled trial

Faculty of Medicine, Chulalongkorn University0 个研究点目标入组 120 人开始时间: 2021年10月21日最近更新:
适应症

试验速览

阶段
4 期
入组人数
120

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
18 Years 至 65 Years(—)
性别
All

入选标准

  • 1. Scheduled for elective open upper abdominal surgery
  • 2. General anesthesia combined with thoracic epidural anesthesia.
  • 3. Age 18-65 years old
  • 4. American Society of Anesthesiology (ASA) Physical Status class 1-3

排除标准

  • 1. Patients who refused to participate in the study.
  • 2. Patients with contraindications and a history of allergy with drugs used in the study.
  • 3. Patients who are contraindicated for epidural analgesia are:
  • 4. Patients with neurologic disorder.
  • 5. Patients with chronic pain
  • 6. Inadequate epidural analgesia after surgery
  • 7. Patients who are unable to use the patient-controlled epidural analgesia

研究者

相似试验