NCT04720287已完成4 期
Ultrasound Guided Quadratus Lumborum Block Compared to Caudal Bupivacaine/ Neostigmine in Pediatric Lower Abdominal Surgeries, a Randomized Controlled Trial
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- The total amount of paracetamol doses (mg)
研究概览
简要总结
The aim of this study is to compare the postoperative pain control in children undergoing lower abdominal surgeries receiving QL block with those receiving caudal bupivacaine/ neostigmine.
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
- Double (Participant, Care Provider)
入排标准
- 年龄范围
- — 至 15 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients American Society of Anesthesiologists physical status (ASA) I or II.
- •Consent from parents or legal guardian(s).
- •Lower abdominal surgeries.
排除标准
- •Parents' refusal or legal guardian's refusal.
- •Infection at the injection site.
- •Known allergy to bupivacaine and/or neostigmine.
- •Contraindications to regional anesthesia (including coagulopathy and local infection).
- •Anatomical anomalies at the site of the block.
研究组 & 干预措施
Group 1(QL group)
Active Comparator
干预措施: bupivacaine/ neostigmine. (Drug)
Group 2 (CB group)
Active Comparator
干预措施: bupivacaine/ neostigmine. (Drug)
结局指标
主要结局
The total amount of paracetamol doses (mg)
时间窗: 24 hours postoperatively
The total amount of paracetamol doses (mg)
次要结局
未报告次要终点
研究者
Dr.Ibrahim Mamdouh Esmat
Assistant Professor of Anesthesia and Intensive Care Department, Faculty of Medicine, Ain- shams University, Cairo, Egypt.
Ain Shams University
研究点 (1)
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