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临床试验/NCT04215614
NCT04215614已完成不适用

The Comparison of Lateral Sagittal vs Costoclavicular Brachial Plexus Block in Children

Ataturk University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2020年1月2日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
Block performance time

研究概览

简要总结

Costoclavicular approach has lots of advantages compared to the lateral sagittal approach for infraclavicular brachial plexus block. Although the efficacy of this block has been demonstrated in adults, there are no randomized controlled trials in the literature on the application of pediatric patients. Our aim was to compare the ultrasound-guided infraclavicular and costoclavicular approach in pediatric patients.

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
Single (Participant)

入排标准

年龄范围
5 Years 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • American Society of Anesthesiologist's physiologic state I-II patients
  • Patients who will undergo hand or forearm surgery

排除标准

  • Infection in the area to be injected
  • Coagulopathy,
  • Previously known neurological damage

研究组 & 干预措施

Group Lateral Sagittal

Active Comparator

Ultrasound-Guided lateral sagittal brachial plexus block with 1:1 ratio 2% lidocaine, and 0.5% bupivacaine

干预措施: Lidocaine and Bupivacaine solution (Drug)

Group Lateral Sagittal

Active Comparator

Ultrasound-Guided lateral sagittal brachial plexus block with 1:1 ratio 2% lidocaine, and 0.5% bupivacaine

干预措施: Lateral Sagittal block (Device)

Group Costoclavicular

Active Comparator

Ultrasound-Guided costoclavicular brachial plexus block with 1:1 ratio 2% lidocaine, and 0.5% bupivacaine

干预措施: Lidocaine and Bupivacaine solution (Drug)

Group Costoclavicular

Active Comparator

Ultrasound-Guided costoclavicular brachial plexus block with 1:1 ratio 2% lidocaine, and 0.5% bupivacaine

干预措施: Costoclavicular block (Device)

结局指标

主要结局

Block performance time

时间窗: Twenty minutes before surgery

The time interval between the contact of the ultrasound probe to skin and end of local anesthetics injection.

次要结局

  • Visual analog pain score(Postoperative 24 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ahmet Murat Yayik

Assistant Professor

Ataturk University

研究点 (1)

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