跳至主要内容
临床试验/CTRI/2018/10/016113
CTRI/2018/10/016113已完成不适用

Postoperative pain relief in Total Knee Arthroplasty: Ultrasound-guided Adductor Canal Block vs Local Intraarticular Infiltration, A Randomised, Prospective, Controlled Trial

All India Institute of Medical Sciences1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2016年4月3日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
To estimate the total morphine consumption in the three groups

研究概览

简要总结

In conclusion, in patients undergoing elective unilateral total knee arthroplasty(TKA), adductor canal block(ACB) was found to be superior to both local intraarticular infiltration and control group in reducing the 24 hour morphine consumption, lowering VAS scores at rest and with movement, prolonging time to first analgesia, reducing requirement of rescue analgesia, lowering worst VAS score during timed up and go test(TUG test) and showing better patient satisfaction scores. The incidence of opioid-related side-effects was comparable among the three groups. Adductor canal block also was not associated with any complications related to its technique, hence ACB can be considered a safe technique to be used in patients undergoing unilateral TKA for postoperative analgesia. While local intra-articular infiltration was found to be superior to control group in reducing 24 hour PCA morphine consumption, lowering VAS scores both at rest and with movement, prolonging time to first analgesia, reducing the requirement of rescue analgesia and showing better patient satisfaction compared to control group.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Open Label

入排标准

年龄范围
18.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • ASA physical status I-III scheduled for elective primary unilateral knee arthroplasty.

排除标准

  • 1.Age > 80 years 2.ASA IV / V 3.Bilateral / Revision TKA 4.Morbid obesity (BMI ≥ 40 ) 5.History of focal neurological deficit 6.History of sensory or motor disorders of limb to be operated 7.History of allergy to local anaesthetics , clonidine 8.History of regular opioid use 9.Local site infection 10.Patient refusal to partake in the study.
  • 11.Contraindication to spinal anaesthesia.

结局指标

主要结局

To estimate the total morphine consumption in the three groups

时间窗: 24 hours postopertively

次要结局

  • To assess pain scores at rest and movement using visual analogue scale(0,4,8,12,24 hours postoperatively)
  • To estimate the time to first use of patient controlled analgesia device(24 hours postoperatively)
  • To compare the side effects associated with morphine consumption in the three groups(24 hours postoperatively)
  • To estimate the worst pain during and time taken to perform the timed get up and go (TUG) test(24 hours postoperatively)
  • To assess patient satisfaction(24 hours postoperatively)

研究者

申办方类型
Government medical college

研究点 (1)

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