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临床试验/NCT01518530
NCT01518530已完成2 期

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

Hillel Yaffe Medical Center2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2012年2月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
10
试验地点
2
主要终点
Occiflex Device Safety

研究概览

简要总结

The study is intended to examine the safety and efficacy of computerized mobilization of the neck for the treatment of patients with chronic neck pain. This is a third continuation study aimed at examining the Occiflex Robotic System. This time we will be studying tailored or personalized three dimensional movement of the neck.

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

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

  • Patients with cervical radiculopathy Myelopathy Discopathy Malignancy involving the neck or cervical spine Severe Osteoporosis Severe skin disorder Psychiatric disorders Cervical disc herniation

结局指标

主要结局

Occiflex Device Safety

时间窗: 6 weeks

A meticulous documentation of any serious adverse effect will be made. Any minor side effects will be recorded with an emphasis on the possible relationship to the treatment. The number of minor and serious adverse effects out of 360 therapeutic sessions will be noted.

次要结局

  • Efficacy as Per the NDI-Neck Disability Index(6 weeks)

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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