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临床试验/CTRI/2019/03/018186
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

AIIMS Bhubaneswar1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年1月4日最近更新:

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

申办方类型
Government medical college

研究点 (1)

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