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临床试验/EUCTR2009-012073-34-NL
EUCTR2009-012073-34-NL进行中(未招募)1 期

Botulinum toxin for treating calf muscle spasticity in Hereditary Spastic Paraparesis (HSP): functional effects on dynamic balance and gait - FEBOCH

Radboud University Nijmegen Medical Centre0 个研究点目标入组 20 人开始时间: 2009年5月6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
20

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
All

入选标准

  • -diagnosis based on molecular diagnosis (e.g. SPG-4 mutations)
  • -age between 18 and 70 years
  • -disabling bilateral calf muscle spasticity (including clonus) without excessive passive stiffness or contracture (i.e. Modified Ashworth Scale 1-3 / 5)
  • -comfortable walking speed greater than 1 km/hr (using a 10m walking test)
  • -being able to stand and walk for 10m without aids
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -impaired tactile and joint motion perception, or cerebellar signs, suggesting ‘complicated’ HSP
  • -other disorders of the neuro-musculo-skeletal system
  • -prior treatment with botulinum toxin or neurolysis of the lower limbs within 6 months
  • -unwillingness or impossibility to keep any oral spasmolytic drugs constant
  • -severe (> 15 degrees) contracture at the knees or hip joints
  • -being unable to load the heels while standing with extended knees (due to ankle contracture)
  • -pregnancy
  • -addiction to drugs or alcohol
  • -any inability to cooperate with the assessments and to give written informed consent

研究者

发起方
Radboud University Nijmegen Medical Centre

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