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临床试验/ISRCTN11851359
ISRCTN11851359已完成不适用

A study to evaluate the feasibility of carrying out a randomised controlled trial to compare the effectiveness of high volume ultrasound guided injections verses eccentric loading exercises in reducing pain and improving function in patients with non-insertional Achilles tendinopathy

niversity of Stirling0 个研究点目标入组 30 人开始时间: 2017年11月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30

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

性别
All

入选标准

  • 1. Male or female
  • 2. Aged 18 or over
  • 3. Capacity to give informed consent
  • 4. Clinical diagnosis of unilateral non- insertional Achilles tendinopathy / plus diagnostic ultrasound confirmation. Clinical diagnosis would include the following:
  • 4.1. Pain and tenderness on palpation of the Achilles tendon 2-6cm from the insertion in to the calcaneus.
  • 4.2. Evidence of tendon thickening on palpation of the Achilles tendon.
  • 4.3. Negative Simmonds-Thompson test.
  • 4.4. Painful arc test
  • 5. English is first language

排除标准

  • 1. Concurrent musculoskeletal ankle problems.
  • 2. Have a diagnosed rheumatological disorder.
  • 3. Suffered partial /complete tear of the Achilles tendon
  • 4. Previous injection for non- insertional Achilles tendinopathy
  • 5. Previous surgery to the Achilles tendon.
  • 6. Patients with bilateral non insertional Achilles tendinopathy.
  • 7. Currently taking quinolone antibiotics
  • 8. Previous allergy to local anaesthesia.
  • 9. English is not the first language

研究者

发起方
niversity of Stirling

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