CTRI/2010/091/001215已完成不适用
Comparision two different doses of caudal clonidine in combination with a single large per rectal dose of paracetamol for post operative pain relief in children - A prospective, randomized double-blind study.
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- AIIMS
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Pain score post operatively - Visual Analogue Scale in >5yrs age group, Modified Objective Pain Score in <5yrs age group
研究概览
简要总结
A prospective randomized double-blind study comparing Clonidine in caudal block in two different doses (1mcg/kg Vs 2mcg/kg)together with Bupivacaine 0.25%,1ml/kg in combination with a single 30 to 40 mg/kg per rectal dose of paracetamol for post operative pain relief in children undergoing elective surgery in infraumbilical regions.
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 2.00 Year(s) 至 8.00 Year(s)（—）
- 性别
- All
入选标准
- •Age 2-8 years, 2)ASA status 1 or 2, 3)Elective surgery in lower abdomen, genitourinary and lower limb regions.
排除标准
- •Refusal by parents or guardians,2)Children undergoing ano-rectal surgeries,3)Presence of renal or liver dysfunction,4)Presence of spinal deformities,5)History of allergy to local anaesthetics,6)History of bleeding disorder,7)Presence of local infection at the site of block.
结局指标
主要结局
Pain score post operatively - Visual Analogue Scale in >5yrs age group, Modified Objective Pain Score in <5yrs age group
时间窗: Upto 24 hours post operative period
次要结局
- Adverse effects of Clonidine if occurs(Upto 24 hours post operative period)
研究者
研究点 (1)
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