跳至主要内容
临床试验/CTRI/2024/06/069175
CTRI/2024/06/069175尚未招募4 期

Analgesic Efficacy of Iliopsoas Plane Block in Total Hip Arthroplasty : A Randomised Controlled Trial

All India Institute of Medical Sciences, Patna1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2024年6月30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
56
试验地点
1
主要终点
To compare the postoperative opioid consupmtion with and without iliopsoas plane 24hr post operatively

研究概览

简要总结

Total hip arthroplasty is a major orthopaedic procedure associated with significant postoperative pain. Many regional anaesthetic techniques are available to reduce postoperative pain and opioid consumption, most of it causes  motor weakness.

Iliopsoas plane block is a recently developed motor sparing regional anaesthesia technique the targets the sensory branches from the femoral and accessory obturator nerve there by increases the patient outcome in terms of recovery, early mobilisation and satisfaction. There is lack of enough evidence for analgesic efficacy of iliopsoas plane block.

In this study we compare the 24hr post operative opioid consumption with and without iliopsoas plane block in patients undergoing total hip arthroplasty under general anaesthesia

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Outcome Assessor Blinded

入排标准

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

入选标准

  • Patients planned for total hip arthroplasty ASA I, II, III patients Age group 20- 70 years.

排除标准

  • Patient refusal ASA IV High risk patients who may require post operative ICU care Infection over target site Bleeding diathesis Allergic to local anaesthetic.

结局指标

主要结局

To compare the postoperative opioid consupmtion with and without iliopsoas plane 24hr post operatively

时间窗: At 1hr, 6hr, 12hr, 24hr postoperatively

次要结局

  • Post operative time to 1st rescue analgesia(from the time of administration of block to the first need of resue analgesic administration)
  • NRS score at 1hr 6hr 12hr 24hr postoperatively(At 1hr, 6hr, 12hr, 24hr postoperatively)
  • Muscle power at 1hr 6hr 12hr 24hr postoperatively(At 1hr, 6hr, 12hr,24 hr postoperatively)
  • Patient satisfaction(24 hr postoperatively)
  • Postoperative nausea and vomiting(24 hr postoperatively)

研究者

发起方
All India Institute of Medical Sciences, Patna
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Ashmi Latheef

AIIMS PATNA

研究点 (1)

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