跳至主要内容
临床试验/EUCTR2017-002815-32-BE
EUCTR2017-002815-32-BE进行中(未招募)1 期

The dose response of Dexamethasone as perineural adjuvant in Brachial Plexus Block. - DXMPN2017

AZ Groeninge0 个研究点目标入组 75 人开始时间: 2017年7月20日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
AZ Groeninge
入组人数
75

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

  • All patients presenting for elective arthroscopic shoulder surgery (incl. decompression and cuff repairs), aged 18-85 years willing to sign informed consent.
  • 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 75
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Contraindications for brachial plexus blocks: coagulopathies, severe bronchopulmonary disease, intolerance to the study medication, pre-existing neuropathies, infection in the region of the interscalene groove.
  • Weight <50kg
  • Systemic glucocorticoid use
  • Chronic use of opioids
  • History of addiction
  • Oncologic history with chemotherapy (Taxol, Vincristine etc.)
  • Known polyneuropathy
  • Surgery or radiation therapy of the neck
  • Impossibility to understand and sign the informed consent
  • Refusal of the patient

研究者

发起方
AZ Groeninge

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