跳至主要内容
临床试验/CTRI/2025/08/092600
CTRI/2025/08/092600尚未招募2/3 期

Comparison of ultrasound guided femoral triangle block and adductor canal block for postoperative analgesia in total knee arthroplasty

Vardhman Mahavir medical college and Safdarjung hospital1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年8月18日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
To compare the analgesic efficacy of ultrasound guided Femoral triangle block and adductor canal block for pain relief using the numerical rating score(NRS) at rest in patients undergoing total knee arthroplasty

研究概览

简要总结

This study is a prospective interventional randomized comparative trial, Comparing the ultrasound guided Femoral triangle block ( 15 ml of 0.25 % bupivacaine and 30 mcg clonidine) and adductor canal block ( 15 ml of 0.25% bupivacaine and 30 mcg clonidine) in patients undergoing total knee arthroplasty under subarachnoid block in a single centre in India. The primary outcome will be measured using Numerical rating score (NRS) postoperatively.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator, Outcome Assessor and Date-entry Operator Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Patients aged 18-65 years with American Society of Anesthesiologists physical status I-III scheduled for elective unilateral Total Knee Arthroplasty.

排除标准

  • Contraindications to Femoral Triangle and Adductor Canal Block.
  • Patients receiving opioids for chronic analgesic therapy.
  • Contraindication to Subarachnoid Block.
  • Inability to comprehend Numeric Rating Scale.

结局指标

主要结局

To compare the analgesic efficacy of ultrasound guided Femoral triangle block and adductor canal block for pain relief using the numerical rating score(NRS) at rest in patients undergoing total knee arthroplasty

时间窗: At 2 hours postoperatively

次要结局

  • NRS at rest(At 0, 1, 4, 8 and 24 hours)
  • NRS on movement(At 24 hours)
  • Time to first rescue analgesia
  • Total analgesic consumption postoperatively(In first 24 hours)
  • Quadriceps muscle strength using Bromage scale(At 24 hours postoperatively)

研究者

发起方
Vardhman Mahavir medical college and Safdarjung hospital
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Lohith H T

Vardhman Mahavir medical college and Safdarjung hospital

研究点 (1)

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