A STUDY COMPARING CAUDAL BLOCK AND PENILE BLOCK USING ROPIVACAINE FOR POST OPERATIVE ANALGESIA IN PEDIATRIC PATIENT POSTED FOR CIRCUMCISION
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- To compare the duration of caudal block and penile block using ropivacaine for postoperative analgesia in pediatric patients posted for circumcision.
研究概览
简要总结
This is a randomized, prospective, single centre study comparing two procedures : caudal block and penile block using the drug Ropivacaine (0.25%) at a dose of 0.2 ml/kg IV for postoperative analgesia in pediatric patients posted for circumcision within 6 months duration in 30 patients ; 15 in each group. All the cases are done in India. The primary outcome is to observe the duration of block and pain relief using Visual Analog Scoring (VAS) and FLACC (Face, Legs, Activity, Crying and Consolability) pain scale scoring.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 1.00 Year(s) 至 7.00 Year(s)（—）
- 性别
- Male
入选标准
- •ASA grade I and ASA grade II fit patients.
- •Hemodynamically stable patients with all routine investigations within normal limits and without any other co-morbidities.
- •Availability of written and informed consent and willingness of the parent to be a part of the study.
排除标准
- •1.Patients with ASA physical status III or more.
- •2.Patients posted for emergency procedures.
- •3.Patients with major neurological, cardiac, respiratory, renal, hepatic or coagulation abnormalities.
- •4.Patients having history of hypersensitivity to local anesthetic and opioids.
- •5.Patients having any contraindications to caudal block or penile block.
- •6.Patients having known fetal abnormalities.
结局指标
主要结局
To compare the duration of caudal block and penile block using ropivacaine for postoperative analgesia in pediatric patients posted for circumcision.
时间窗: Monitored for vitals and analgesia for 24 hours postoperatively using VAS scoring more than 7 and FLACC scoring more than 5
次要结局
- To compare the following:(1. To evaluate the duration of the block postoperatively.)