Comparison of Analgesic Efficiency of Pudendal Nerve Block and Penil Block for Circumsion in Children
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 80
- 主要终点
- Postoperative pain evaluatiom
研究概览
简要总结
The aim of this prospective randomized study is to assess the analgesic efficacy of Pudendal block compared with penil block for pediatric patients undergoing circumsion concerning postoperative analgesic consumption within 24 hours.
详细描述
In this prospective study, patients will be randomized into 2 groups, either receiving penil Block( PNL) or nerve stimulator-guided Pudendal Nerve Block(PNB). Analgesic consumption will be assessed during the first 24 hours postoperatively. The "CHEOPS pain scale" will use to assess postoperative pain.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Care Provider, Outcomes Assessor)
入排标准
- 年龄范围
- 1 Year 至 12 Years（Child）
- 性别
- Male
- 接受健康志愿者
- 是
入选标准
- •ASA I-II patients, aged 1-12 years old patient undergoing circumcision,
排除标准
- •history of local anesthetics's allergy, infection at the injection side, anatomical abnormalities, coagulopaty, bleeding disease, liver disease
研究组 & 干预措施
Pudendal block group in circumcision
Nerve stimulated pudendal nerve block performed under general anesthesia
干预措施: penil or pudendal nerve block in circumcision (Procedure)
Penil block group in circumcision
Penil block performed by surgeon under general anesthesia
干预措施: penil or pudendal nerve block in circumcision (Procedure)
结局指标
主要结局
Postoperative pain evaluatiom
时间窗: 24 hour
CHEOPS pain scale
次要结局
未报告次要终点
研究者
Ayse Cigdem Tutuncu
assoc prof
Istanbul University