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临床试验/EUCTR2015-003587-36-GB
EUCTR2015-003587-36-GB进行中(未招募)1 期

Chronic Tendinopathy: The Biomechanical Associations and EfFicacy of Injectable Therapy (BE FIT) Study - Biomechanical Associations & EfFicacy of IInjectable Therapy (BE FIT)

Directorate of Defence Rehabilitation0 个研究点目标入组 108 人开始时间: 2016年2月19日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
108

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Male

入选标准

  • Chronic Achilles and patella tendinopathy patients
  • No or minimal improvement with physical rehabilitation pathway outlined below
  • Minimum duration of symptoms of 6 months
  • US evidence of neovascularization
  • Patients must be medically downgraded and not deployable
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 108
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range 0

排除标准

  • Concurrent alternate lower limb diagnosis
  • Anticoagulant medication
  • Previous tendon surgery or injection

研究者

发起方
Directorate of Defence Rehabilitation

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