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临床试验/NCT01216566
NCT01216566Unknown1 期

Computerized Mobilization of the Cervical Spine Utilizing the Occiflex Device for the Treatment of Chronic Neck Pain

Hillel Yaffe Medical Center1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2010年12月1日最近更新:
适应症
干预措施

试验速览

阶段
1 期
入组人数
10
试验地点
1
主要终点
Safety of computerized continuous mobilization of the cervical spine

研究概览

简要总结

The purpose of this study is to investigate the efficacy and safety of the Occiflex device in the treatment of neck pain.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with chronic neck pain: post-whiplash injury, myofacial pain, cervical facet joint disease and idiopathic chronic neck pain

排除标准

  • •Radiculopathy
  • •Myelopathy
  • •Cerebral vascular disease
  • •Malignancy
  • •Osteoporosis
  • •Cervical disc herniation

研究组 & 干预措施

I. Patients with chronic neck pain

Experimental

干预措施: Occiflex Device (Device)

结局指标

主要结局

Safety of computerized continuous mobilization of the cervical spine

时间窗: one year

次要结局

  • Efficacy of computerized mobilization of treatment of patients with chronic neck pain(one year)

研究者

申办方类型
Other Gov

研究点 (1)

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