跳至主要内容
临床试验/CTRI/2023/10/058647
CTRI/2023/10/058647尚未招募4 期

A randomised controlled, Double blinded study on Ultrasound guided Continuous Suprainguinal Fascia Iliaca block infusion vs Continuous Femoral Nerve block infusion for postoperative analgesia in patients undergoing Total Hip Arthroplasty done under General Anaesthesia

SRM INSTITUTES FOR MEDICAL SCIENCE1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2023年11月15日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
80
试验地点
1
主要终点
TO STUDY THE POSTOPERATIVE ANALGESIA IN GROUP A AND GROUP B

研究概览

简要总结

I about to do a study comparing continuous infusion of suprainguinal fascia iliaca block and  femoral nerve block for  postoperative pain using Visual analog scale score  ,quadriceps muscle strength using MRC grading and rescue analgesic requirement tramadol 1mg/kg in patients undergoing total hip arthroplasty done under general anaesthesia by ultrasound guided technique  till 48 hours postoperatively.

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 75.00 Year(s)(—)
性别
All

入选标准

  • 1 ASA GRADE 1 AND 2 2 ALL GENDERS 3 PATIENT ADMITTED FOR TOTAL HIP ARTHROPLASTY 4 PATIENT WILLING TO PARTICIPATE IN THIS STUDY 5 AGE 20-75 YEARS.

排除标准

  • 1 ASA GRADE 3 AND 4 2 AGE<20 YEARS AND >75 YEARS 3 PREGNANT AND LACTATING MOTHERS 4 OBESE INDIVIDUALS WITH BMI MORE THAN OR EQUAL TO 30 5 PATIENTS PARTICIPATING IN ANY OTHER CLINICAL STUDIES 6 PATIENTS ALLERGIC TO LOCAL ANAESTHETICS AND ANY OTHER DRUGS USED IN THIS STUDY 7 PATIENT NOT WILLING TO PARTICIPATE IN THIS STUDY.

结局指标

主要结局

TO STUDY THE POSTOPERATIVE ANALGESIA IN GROUP A AND GROUP B

时间窗: 48HOURS

次要结局

未报告次要终点

研究者

发起方
SRM INSTITUTES FOR MEDICAL SCIENCE
申办方类型
Research institution and hospital

研究点 (1)

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