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临床试验/ACTRN12614000118606
ACTRN12614000118606尚未招募未知

Evaluating Sensory Perception in Cervical Dystonia

The Alfred0 个研究点目标入组 40 人开始时间: 2014年1月30日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Two groups:
  • 1. Cervical dystonia
  • Cervical dystonia as diagnosed by a movement disorders neurologist, aged > 18 years, capable of providing informed consent. The first visit will be held at the end of the botulinum toxin injection cycle, 12 weeks since last injection.
  • 2. control subjects without known neurological disease or chronic pain syndrome

排除标准

  • 1.Complex dystonia phenotype or familial dystonia
  • 2.Presence of neuropathy (including risk factors as detailed below)
  • b.Carpal tunnel syndrome
  • c.Major cardiac/respiratory/renal impairment
  • d.Deranged thyroid function
  • e.Significant B12 deficiency
  • f.Autoimmune disease
  • g. Past history of multiple myeloma, chemotherapy
  • h.Cervical spine pathology/radiculopathy
  • i.Co-existing neurological disease or other movement disorder
  • j.Pregnancy
  • k. Drug and alcohol abuse
  • l.HepB/HepC/HIV
  • 3.Inability to speak English to sufficient degree to provide appropriate consent
  • 4.Clinically diagnosed dementia
  • 5.Clinically significant generalised pain disorders including
  • b.Back pain
  • c.Fibromyalgia
  • d.Bruxism/TMJ dysfunction

研究者

发起方
The Alfred

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