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临床试验/NCT05887778
NCT05887778已完成4 期

Effect of Systematic Dexamethasone on the Duration of Supraclavicular Brachial Plexus Block for Anesthesia After Pediatric Hand/Wrist Surgery

Poznan University of Medical Sciences2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2023年9月18日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
90
试验地点
2
主要终点
first need of opiate

研究概览

简要总结

Effect of Systematic Dexamethasone on the Duration of Supraclavicular Brachial Plexus Block for Anesthesia After Pediatric Hand/Wrist Surgery

详细描述

This study is proposed to explore the effect of systemic Dexamethasone on the duration of supraclavicular brachial plexus block for analgesia after pediatric ankle surgery.

After hand and wrist surgery, children need good analgesia. Peripheral nerve blocks have provided a safe, effective method to control early postoperative pain when symptoms are most severe.

The safety of local anesthesia is essential in children due to the much lower toxicity threshold of local anesthetics. An effective adjuvant, such as Dexamethasone, could allow for a higher dilution of local anesthetics while maintaining and enhancing their analgesic effect.

There is considerable research where intravenous and perineural dexamethasone use has been compared in adults. However, there is a massive lack of research regarding children.

In this study, investigators compare different doses of systemic Dexamethasone. Before the anesthesia, the patients receive Dexamethasone intravenously. Groups 2 and 3 have dexamethasone doses of 0.1mg/kg and 0.2mg/kg.

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, Care Provider, Investigator)

入排标准

年龄范围
3 Months 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • children scheduled for hand/wrist surgery
  • body weight > 5kg

排除标准

  • infection at the site of the regional blockade
  • coagulation disorders
  • immunodeficiency
  • ASA= or >4
  • steroid medication in regular use

研究组 & 干预措施

placebo injection

Active Comparator

5ml of 0,9% sodium chloride - before the popliteal nerve block

干预措施: Sodium Chloride 0.9% Inj (Drug)

0,1mg/kg Dexamethasone

Active Comparator

0,1mg/kg dexamethasone sodium phosphate - before the popliteal nerve block

干预措施: 0,1mg/kg Dexamethasone (Drug)

0,2 mg/kg Dexamethasone

Active Comparator

0,2 mg/kg dexamethasone sodium phosphate - before the popliteal nerve block

干预措施: 0,2mg/kg Dexamethasone (Drug)

结局指标

主要结局

first need of opiate

时间窗: 48 hours

Time after surgery when the patient needs opiate for the first time

次要结局

  • NLR(24 and 48 hours after surgery)
  • Blood glucose(24 and 48 hours after surgery)
  • Opioid Consumption(48 hours)
  • Pain score(4 hours, 8 hours, 12 hours, 16 hours, 18 hours, 24 hours, 28 hours, 32 hours, 36 hours, 40 hours, 44 hours, 48 hours after surgery)
  • PLR(24 and 48 hours after surgery)
  • Mobilisation(4 hours, 8 hours, 12 hours, 16 hours, 18 hours, 24 hours, 28 hours, 32 hours, 36 hours, 40 hours, 44 hours, 48 hours after surgery)

研究者

发起方
Poznan University of Medical Sciences
申办方类型
Other
责任方
Sponsor

研究点 (2)

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