跳至主要内容
临床试验/EUCTR2013-002359-14-AT
EUCTR2013-002359-14-AT进行中(未招募)不适用

ltrasound Guided Caudal Blockade in Children between 30 and 50kg: A Feasibility Study - Caudal block study 30-50kg

Medizinische Universität Wien, Universitätsklinik für Anästhesie, Allgemeine Intesnivmedizin und Schmerztherapie0 个研究点开始时间: 2013年9月20日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Patients between 30 and 50 kg bodyweight undergoing subumbilical surgery
  • Written informed consent given by the parents/child after being provided with detailed information about the nature, risks, and scope of the clinical study as well as the expected desirable and adverse effects.
  • No legal incapacity and/or other circumstances rendering the parents/child unable to understand the nature, scope and possible consequences of the study
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 20
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Parents or Child’s refusal
  • Coagulopathy or anticoagulation therapy
  • Suspicion of increased intracranial pressure
  • Known allergy or hypersensitivity against Ropivacaine or amino-amide local anaesthetics
  • Anatomical abnormalities of the limb or lower spine region
  • Participation in another clinical study within the last 4 weeks prior to study
  • Abnormalities in ECG that are considered clinically relevant such as AV-block or bradycardia
  • Other objections to participate in the study in the opinion of the investigator
  • Study Protocol / Methods

研究者

发起方
Medizinische Universität Wien, Universitätsklinik für Anästhesie, Allgemeine Intesnivmedizin und Schmerztherapie

相似试验