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临床试验/2023-506062-31-00
2023-506062-31-00撤回4 期

Comparison of different doses of perineural dexmedetomidine as adjuvans to ropivacaine 0,67% for interscalene plexus block in association with 10 mg intravenous dexamethasone: a single center, double blinded, randomised controlled trial.

Algemeen ziekenhuis Rivierenland1 个研究点 分布在 1 个国家目标入组 260 人开始时间: 2023年8月16日最近更新:

试验速览

阶段
4 期
状态
撤回
发起方
入组人数
260
试验地点
1
主要终点
Length of analgesia ( time untill intake of analgeticum )

研究概览

简要总结

To look at the efficacy of different doses of perineural dexmedetomidine to prolong the length of the analgetic block after a interscalene plexus block.

入排标准

年龄范围
18 years 至 65+ years(18-64 Years, 65+ Years)
接受健康志愿者

入选标准

  • Patients scheduled for elective shoulder surgery

排除标准

  • Chronic pain
  • Contra-indications for peripheral nerve block
  • Allergy for ropivacaine, dexmedetomidine or dexamethasone
  • > 80 years old
  • second degree AV block
  • Emergency operations
  • No informed consent
  • Medical history of cardial, renal or hepatic failure
  • Dehydratation
  • Neurologic deficits or neuropathia of the brachial plexus

结局指标

主要结局

Length of analgesia ( time untill intake of analgeticum )

Length of analgesia ( time untill intake of analgeticum )

次要结局

  • Lenght of sensoric block
  • Length of motoric block
  • Percentage of postoperative nausea and vomiting first 48 hours
  • Time to recovery after anesthesia
  • Percentage of side effects during anesthesia ( hypotension, bradycardia )
  • Numeric Rating Scale score for pain the first 48 hours
  • Cumulative opioid consumption over 48 hours

研究者

发起方
Algemeen ziekenhuis Rivierenland
申办方类型
Health care
责任方
Principal Investigator
主要研究者

herve vanden eede

Scientific

Algemeen ziekenhuis Rivierenland

研究点 (1)

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