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
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
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