Comparison of caudal anaesthesia and ilioinguinal block for paediatric inguinal surgeries and post operative analgesia
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- 1. Efficacy and quality of postoperative analgesia
研究概览
简要总结
This will be a randomized prospective study which will be done to compare caudal anaesthesia and ilioinguinal block for paediatric inguinal surgeries and postoperative analgesia. The study will be carried out in 60 children of ASA grade I and II who will be divided into two groups of 30 each. Group A will be given caudal block, group B will be given illioinguinal/illiohypogastric block, both using combination of ropivacaine and dexmedetomidine. Both groups will be compared with respect to effect on efficacy and duration of postoperative analgesia and any complication if seen. The observations will be recorded on the proforma and the results will be statistically analysed in two groups.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 3.00 Year(s) 至 12.00 Year(s)（—）
- 性别
- All
入选标准
- •Children belonging to ASA group I/II
- •Age range between 3-12 years of either sex.
排除标准
- •Children belonging to ASA Grade 3 and 4
- •Children with history of coagulation disorders such as hemophilia, ITP, tumors or DIC
- •Active infection at the site of injection such as cellulitis, abscess, meningitis etc.
- •Unstable BP or heart rate
- •Patient or parent refusal
- •Scoliosis
- •Congenital anomaly of spinal cord or vertebral bodies
- •Relatively contraindicated in patients with decreased cardiac function and in patients with muscular dystrophy.
结局指标
主要结局
1. Efficacy and quality of postoperative analgesia
时间窗: 12 hours
2. Duration of postoperative analgesia
时间窗: 12 hours
次要结局
- Complications(1-24 hours)