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临床试验/EUCTR2015-001559-55-BE
EUCTR2015-001559-55-BE进行中(未招募)1 期

Quality of analgesia after interscalene block with 5 mL of bupivacaine 0.25% and 10 mL of Exparel® (133 mg) vs. 15 mL of 0.25% bupivacaine after arthroscopic shoulder surgery - Exparel-interscalene block study

Ziekenhuis Oost-Limburg, Departement of Anesthesia0 个研究点目标入组 40 人开始时间: 2015年4月30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
入组人数
40

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

  • ?Dutch or English speaking adults
  • ?18 years or older ASA I-III physical class
  • ?Scheduled for elective arthroscopic shoulder surgery
  • 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 30
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 10

排除标准

  • ?History of allergy to a local anesthetic
  • ?Baseline neurological deficit
  • ?Medical condition that would make it difficult to assess sensory distribution or communicate with our staff
  • ?Recent history (< 3 months) of drug or alcohol abuse
  • ?Concomitant opioid therapy
  • ?Preexisting coagulation disorder
  • ?Infection at the injection site

研究者

发起方
Ziekenhuis Oost-Limburg, Departement of Anesthesia

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