跳至主要内容
临床试验/NL-OMON34278
NL-OMON34278已完成3 期

Efficacy of post-operative pain management with intralesional ropivacaine after subacromial decompression - Pain management after subacromial decompression.

Ziekenhuisgroep Twente0 个研究点目标入组 189 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
189

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • Patients (18 years and older) with subacromial impingement syndrome who need a subacromial decompression by dr. C. van Doorn

排除标准

  • Significant damage at the affected shoulder or untreatable subacromial impingement
  • a history of injury at the affected shoulder
  • a history of surgery at the affected shoulder
  • a history of mastectomy at the affected side
  • a neuropathologic condition at the affected shoulder
  • chonic use of opioids
  • extraordinary risk-increasing factors, like morbid obesity
  • Parkinsons disease
  • contraindications for the used medications
  • disability which leads to an inability to describe pain and inability to fill in the VAS score.
  • not understand written and/or spoken Dutch

研究者

发起方
Ziekenhuisgroep Twente

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