跳至主要内容
临床试验/CTRI/2024/07/070165
CTRI/2024/07/070165尚未招募4 期

Compare analgesic efficacy of USG guided pericapsular nerve group block versus suprainguinal fascia iliaca block for post operative pain relief in hip surgery

Department of Anaesthesia and Pain Medicine Pt JNM Medical College Raipur1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年7月8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
Duration of pain relief assessment

研究概览

简要总结

Written informed consent will be taken from  patients undergoing hip surgery under SAB between 25-75 years

Patients will be randomly allocated into two groups

Group A will receive pericapsular nerve group block and Group B will receive suprainguinal fascia iliaca block

To avoid bias patient and observer will be unaware of the type of block given

Time  to first requirement of analgesics will be noted

Total analgesic requirement in 24 hours, VAS score assessment for severity of pain,  patient’s satisfaction score and procedure or drug related complications noted

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Double

入排标准

年龄范围
25.00 Year(s) 至 75.00 Year(s)(—)
性别
All

入选标准

  • ASA 1-3,Patients scheduled for unilateral hip surgery.

排除标准

  • Patient refusal
  • Surgery more than 150 min
  • Coagulation or bleeding disorder
  • Allergy to local anaesthetics
  • Presence of other fracture requiring surgery
  • Morbid obesity
  • Pre-existing uncontrolled cardiovascular disease, renal failure, hepatic failure.

结局指标

主要结局

Duration of pain relief assessment

时间窗: Time to first requirement of analgesics will be noted post operative till 24hours

次要结局

  • 1. Total analgesic requirement in 24 hrs postoperatively.(2.Intensity of pain relief assessment by VAS score at 0,2,4,8,12,24 hours.)

研究者

发起方
Department of Anaesthesia and Pain Medicine Pt JNM Medical College Raipur
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Simran Rana

Pt jnm medical college raipur cg

研究点 (1)

Loading locations...

相似试验