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临床试验/NL-OMON47499
NL-OMON47499已完成3 期

*Effectiveness of Ultrasound Guided Percutaneous treatment of Lateral Epicondylitis using standardized perforation with application of autologous blood, dextrose or perforation only, in relation to pain and functional recovery; A randomized controlled trial * - Ultrasound guided needle therapy in LE

Amphia Ziekenhuis0 个研究点目标入组 165 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
165

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Patients referred by their GP to the orthopaedic surgeon diagnosed with unilateral Lateral Epicondylitis
  • Age between 18 and 70 years
  • Unsuccessful conservative treatment
  • Able to read and write in Dutch
  • Provision of informed consent by patient.

排除标准

  • Prior injection therapy (during this episode of LE), surgery or trauma at the affected elbow
  • Inflammatory diseases (i.e. rheumatoid arthritis, psoriatic arthritis, or reactive arthritis)
  • Patients with any other elbow pathology
  • Neck pain or shoulder pain correlated with elbow pain such as C6 radiculopathy or with disability of the arm or other chronic widespread pain syndromes
  • Traumatic onset of LE.
  • Bilateral LE (mild cases of LE on the contralateral elbow without functional limitations are allowed).
  • Abnormalities on the X-ray.
  • Patients with additional pain at the medial epicondyl.
  • Allergy for lidocaine

研究者

发起方
Amphia Ziekenhuis

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