NCT02678585已完成不适用
Nalbuphine as an Adjuvant to Intravenous Regional Anesthesia
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 106
- 试验地点
- 1
- 主要终点
- Tourniquet and postoperative pain measured by visual analogue scale
研究概览
简要总结
The effect of addition of nalbuphine to lidocaine in intravenous regional anesthesia
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 20 Years 至 50 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •adult patients
- •American Society of Anesthesiologists (ASA) physical status I-II
- •age between 20 and 50 years old
- •scheduled for elective unilateral short hand surgery
排除标准
- •allergy to study medications
- •body mass index > 35 kg/m2
- •patients with sickle cell disease or Reynaud disease
- •patient refusal
研究组 & 干预措施
Nalbuphine
Active Comparator
53 patients received intravenous regional lidocaine plus Nalbuphine
干预措施: Nalbuphine (Drug)
Control group
Other
53 patients received intravenous regional lidocaine
干预措施: Lidocaine (Drug)
结局指标
主要结局
Tourniquet and postoperative pain measured by visual analogue scale
时间窗: 4 hours
次要结局
- Cortisol level(4 hours)
研究者
Mohamed Bakri
Associate professor
Assiut University
研究点 (1)
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