跳至主要内容
临床试验/EUCTR2015-002958-12-NL
EUCTR2015-002958-12-NL进行中(未招募)不适用

Median Local Anaesthetic dose (MLAD) of Intrathecal Bupivacaine in total hip arthroplasty with the anterior approach.

Reinier de Graaf Groep0 个研究点开始时间: 2015年7月20日最近更新:
适应症
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

  • In order to be eligible to participate in this study, a subject must meet all of the following criteria:
  • * ASA I to III
  • * 18y or older
  • * Primary uncemented THA with anterior approach
  • * Willing to participate
  • * Speaking Dutch language
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 10
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 15

排除标准

  • A potential subject who meets any of the following criteria will be excluded from participation in this study:
  • * Hypersensitivity to local anesthetics or any of the other excipients of Bupivacaine
  • * Any other contraindications relate to intrathecal anesthesia
  • * CNS disease, e.g. meningitis, tumor, poliomyelitis, cerebral haemorrhage
  • * Spinal stenosis and diseases or recent trauma to the cervical column
  • * Pernicious anemia with symptoms related to cervical degradation
  • * Pyogenic infections of the skin close to the injection site
  • * Cardiogenic or hypovolemic shock
  • * Disturbance in coagulation or treatment with anti-coagulants
  • * Patient is participating in a medicinal study
  • * Noncompliant with intrathecal anesthesia

研究者

发起方
Reinier de Graaf Groep

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