跳至主要内容
临床试验/NCT04292782
NCT04292782已完成不适用

Caudal Epidural Block Compared to Anterior Quadratus Lumborum Block for Pediatric Hip Surgery

University Tunis El Manar2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2020年3月31日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40
试验地点
2
主要终点
analgesics consumption

研究概览

简要总结

Caudal blockade (CB) is one of the most frequently performed regional anaesthetic techniques in children. It's an efficient way to offer perioperative analgesia for painful sub-umbilical interventions but with high incidence of motor block and urinary retention. In one study, psoas compartment block was associated with less morphine comsumption and prolonged duration of analgesia compared to single-shot caudal Block in small children undergoing open hip reduction/osteotomies. Ultasound guided anterior Quadratus lumborum block (AQLB) provides unilateral analgesia to the nerves between the psoas muscle (PM) and the quadratus lumborum muscle (QLM). The first pediatric study evaluating Quadratus lumborum block is encouraging .

The first pediatric study evaluating Quadratus lumborum block is encouraging. To the best of the investigator's knowledge, there are no previously published data comparing the AQLB with other regional techniques in infants undergoing hip surgery.

详细描述

The aim of this prospective randomized study was to compare the analgesic effects between AQLB and CB in children undergoing unilateral open hip reduction/osteotomies for hip dislocation.

Patients were randomly assigned, into 1 of 2 groups, namely, group CB (n = 20) and group AQLB (n = 20).

Preoperatively all children were premedicated by using oral midazolam (0 .5mg/kg).

anesthesia was induced with 3 to 4% sevoflurane and 50% with 60% nitrous oxide in oxygen.Then fentanyl 3 μg/kg and Propofol 1 - 2mg/Kg were administered for anesthesia induction. Airway was secured with endotracheal tube placed in the mouth facilited by 0.15 mg/kg cistracurium. Anesthesia maintenance was performed with sevoflurane 2% in 50% nitrous oxide.

AQLB and CB were done with 1 ml/kg, 0.25% Ropivacaine (maximum dose limited to 20 ml)

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
2 Years 至 7 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Patients aged 2 to 7 years old
  • Weight ≤ 20 Kg
  • American Society of Anesthesiologists (ASA) physical status I or II
  • Planned to undergo unilateral open hip reduction/osteotomies

排除标准

  • Cerebral palsy with severe intellectual disability
  • Coagulation disorders
  • Local or general infection
  • Allergy to amide local anesthetics.
  • Progressive neurological disorders
  • Parenteral refusal
  • Spinal dysraphism
  • Cutaneous anomalies (angioma, hair truft, naevus or a dimple)near to the puncture

结局指标

主要结局

analgesics consumption

时间窗: day one

total tramadol consumption

次要结局

  • analgesic rescue(Day one)
  • postoperative pain score(day one)

研究者

发起方
University Tunis El Manar
申办方类型
Other
责任方
Principal Investigator
主要研究者

Olfa kaabachi, MD

Professor

University Tunis El Manar

研究点 (2)

Loading locations...

相似试验