CTRI/2019/03/018186尚未招募4 期
Comparison of analgesic efficacy of continuous intravenous infusion versus intermittent bolus of paracetamol in postoperative pain relief following laparoscopic cholecystectomy : A randomized control trial
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Reduction in VAS score by 30% in the first 24hours postoperatively
研究概览
简要总结
This is a randomised controlled trial comparing the analgesic efficacy of continuous intravenous infusion versus intermittent bolus of paracetamol in postoperative pain relief in the first 24 hours following laparoscopic cholecystectomy. The primary outcome measures will be reduction in VAS (Visual Analogue Score) during the first 24 hrs post-operatively. The amount of rescue analgesic consumed will also be assessed.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Double Blind Double Dummy
入排标准
- 年龄范围
- 20.00 Year(s) 至 65.00 Year(s)(—)
- 性别
- All
入选标准
- •ASA I and II Elective laparoscopic cholecystectomy patients.
排除标准
- •Allergy to paracetamol Psychiatric patient Patients on benzodiazepine therapy Deranged liver function test Emergency laparoscopic cholecystectomy patients Alcoholics.
结局指标
主要结局
Reduction in VAS score by 30% in the first 24hours postoperatively
时间窗: VAS score will be assessed post-operatively at hourly interval for the first 4 hours and then 8 hourly upto 24 hours, or on need basis
次要结局
- Amount of rescue analgesics required in the first 24 hrs postoperatively(24 hrs)
研究者
研究点 (1)
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