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临床试验/ACTRN12620000035921
ACTRN12620000035921已完成未知

The efficacy of radial shockwave therapy compared with sham shockwave therapy in insertional Achilles tendinopathy. A randomised controlled trial

Monash University0 个研究点目标入组 76 人开始时间: 2020年1月21日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
76

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Aged 18 years or older
  • >3 months of pain at the insertion of the Achilles to the posterior calcaneal surface
  • Primary complaint of insertional Achilles pain on one or both lower limbs
  • Clinical diagnosis of insertional Achilles tendinopathy based on the following criteria:
  • oGradual onset pain in the relevant area;
  • oPain during or after Achilles tendon loading activities (e.g. walking, running)
  • Ankle joint examination is normal and passive plantar-flexion is painfree;
  • Confirm diagnosis with ultrasound imaging of the Achilles tendon. One or more of the following features present in the insertion area: (i) thickening of the anteroposterior tendon insertion; and/or (ii) hypoechoic regions with or without thickening/fluid within the retrocalcaneal bursa

排除标准

  • Previous rSWT treatment for any condition
  • Previous Achilles tendon surgery in the most symptomatic Achilles tendon
  • Previous Achilles tendon rupture in the most symptomatic Achilles tendon
  • Other ankle conditions including impingement syndrome or any midportion Achilles symptoms that are worse than the insertional Achilles pain
  • Tendinopathy caused by inflammatory conditions (e.g. ankylosing spondylitis)
  • Neurological disorders (i.e. Parkinson’s syndrome, stroke)
  • Inherited connective tissue disorders (i.e. Ehlers- Danlos syndrome, Marfan’s syndrome)
  • Use of fluoroquinolone antibiotics within the previous two years
  • Injection of local anaesthetic, corticosteroid, platelet rich plasma or other pharmaceutical agent into the Achilles tendon or surrounding area within the previous three months
  • Any medical and/or social reason that, in the opinion of the investigators, makes the participant unsuitable for inclusion
  • Serious mental health problem that would preclude adherence to study or treatment protocols

研究者

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