NCT02618876已完成不适用
Nalbuphine as an Adjuvant to Caudal Bupivacaine for Postoperative Analgesia in Children Undergoing Hypospadias Repair
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
- 60
- 试验地点
- 1
- 主要终点
- Postoperative pain intensity Measured by Face, Legs, Activity, Cry & consolability (FLACC) pain scale
研究概览
简要总结
Nalbuphine as an adjuvant to bupivacaine caudal anesthesia for postoperative analgesia in children undergoing Hypospadias repair.
2 groups, 30 patients each
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
- 2 Years 至 10 Years(Child)
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •Children undergoing elective Hypospadias repair
- •with American Society of Anesthesiologists (ASA) physical status I
- •age 2-10 years
排除标准
- •Coagulation disorder
- •allergy to study medications
- •major malformations of the lower spine or meninges or any cutaneous or subcutaneous lesion at the site of injection.
研究组 & 干预措施
Nalbuphine group
Active Comparator
30 children will be given Caudal Bupivacaine plus Nalbuphine.
干预措施: Nalbuphine plus Bupivacaine (Drug)
Control group
Other
30 children will be given Caudal Bupivacaine.
干预措施: Bupivacaine (Drug)
结局指标
主要结局
Postoperative pain intensity Measured by Face, Legs, Activity, Cry & consolability (FLACC) pain scale
时间窗: During 24 h in the postoperative period
次要结局
- Cortisol level(6 hours)
研究者
Mohamed Bakri
Associate professor
Assiut University
研究点 (1)
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