NCT01216566
Unknown
Phase 1
Computerized Mobilization of the Cervical Spine Utilizing the Occiflex Device for the Treatment of Chronic Neck Pain
ConditionsNeck Pain
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Neck Pain
- Sponsor
- Hillel Yaffe Medical Center
- Enrollment
- 10
- Locations
- 1
- Primary Endpoint
- Safety of computerized continuous mobilization of the cervical spine
- Last Updated
- 15 years ago
Overview
Brief Summary
The purpose of this study is to investigate the efficacy and safety of the Occiflex device in the treatment of neck pain.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients with chronic neck pain: post-whiplash injury, myofacial pain, cervical facet joint disease and idiopathic chronic neck pain
Exclusion Criteria
- •Radiculopathy
- •Myelopathy
- •Cerebral vascular disease
- •Malignancy
- •Osteoporosis
- •Cervical disc herniation
Outcomes
Primary Outcomes
Safety of computerized continuous mobilization of the cervical spine
Time Frame: one year
Secondary Outcomes
- Efficacy of computerized mobilization of treatment of patients with chronic neck pain(one year)
Study Sites (1)
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