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临床试验/NCT06655571
NCT06655571招募中不适用

What Technique for Caudal Block in Children: Conventional or Ultrasound-guided

Tunis University2 个研究点 分布在 1 个国家目标入组 94 人开始时间: 2024年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
94
试验地点
2
主要终点
Success rate of block

研究概览

简要总结

The goal of our study is to compare ultrasound-guided caudal block to the conventional technique based on anatomical landmarks.

详细描述

The primary endpoint was the success rate of each technique. We also collected the time taken for each technique, the number of punctures, and the incidence of complications (subcutaneous infiltration, intravascular injection).

Children were randomized to receive a caudal block based on anatomical landmarks (group C) or ultrasound-guided (group E) at a dose of 1 ml/kg of 0.25% bupivacaine, not exceeding 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
Other
盲法
None

入排标准

年龄范围
6 Months 至 6 Years(Child)
性别
All
接受健康志愿者

入选标准

  • children aged between 6 months and 6 years, ASA 1 , underwent elective surgery

排除标准

  • severe systemic diseases, previous neurological or spinal disorders, coagulation abnormalities, allergies toward LAs, local infection at the block site

结局指标

主要结局

Success rate of block

时间窗: during surgery

A successful block was defined as an absence of significant motor movements following surgical induction or aberrations in the heart or respiratory rates

次要结局

  • block performing time(perioperative)
  • number of needle puncture(during procedure)
  • complication rates(during procedure)

研究者

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

Mehdi Trifa

Head of the anesthesia and intensive care department

Tunis University

研究点 (2)

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