跳至主要内容
临床试验/CTRI/2019/10/021787
CTRI/2019/10/021787尚未招募不适用

Effectiveness Of Ultrasound guided Adductor canal block for post operative pain management in below Knee Orthopedics surgery

Elakuchi Vikas Rao1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2019年1月11日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
160
试验地点
1
主要终点
Post- operative VAS(visual analogue Score) and rescue analgesic requirement

研究概览

简要总结

we are going to study the effectiveness of  adductor canal block in the patients who are undergoing below knee orthopaedics surgeries .we will randomly divide patients in to two groups (A &B) by computer generated randomization list . for group A patients ultrasound guided adductor canal block will be given at the end of surgery with 40ml of  0.125% bupivacaine around the sephanous nerve in the middle third of thigh. for group B patients intravenous analgesics will be given post-operatively . for both the groups injection paracetamol 1gm will be given  post-operatively. pain in the post-operative period will be compared by using VAS (visual analogue score) on a scale of 0-10. if score is more than 3 ,as a rescue analgesic tramadol 1mg/kg body wt will be given. After that  VAS will be assessed every 10 minutes and if VAS remains >3 ,an inccremental dose of 0.25mg/kg of tramadol will be given till VAS becomes <3 .The first analgesic demand and total requirement of tramadol in the first 24 hrs will be calculated and compared between both the groups.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • 1.Willing patients operated under spinal anaesthesia.
  • 2.American society of anaesthesiologists (ASA) physical status I and II.
  • 3.Either sex (male/female).
  • Below knee orthopaedic surgeries.

排除标准

  • 1.Patient refusal.
  • 2.History of allergy to the drugs which will be used in the study.
  • 3.Patient enrolled in other studies.
  • 4.Patients with psychiatric disorders.
  • 5.High risk for development of compartmental syndrome.
  • 6.At risk of nerve injury.

结局指标

主要结局

Post- operative VAS(visual analogue Score) and rescue analgesic requirement

时间窗: After the end of surgery till first 24 hours

次要结局

  • Patients feedback on post-operative pain control(After the end of the surgery till first 24 hours)

研究者

发起方
Elakuchi Vikas Rao
申办方类型
Other []

研究点 (1)

Loading locations...

相似试验