Status:
UNKNOWN
Computerized Mobilization of the Cervical Spine Utilizing the Occiflex Device for the Treatment of Chronic Neck Pain
Lead Sponsor:
Hillel Yaffe Medical Center
Collaborating Sponsors:
Headway Ltd.
Conditions:
Neck Pain
Eligibility:
All Genders
18-65 years
Phase:
PHASE1
PHASE2
Brief Summary
The purpose of this study is to investigate the efficacy and safety of the Occiflex device in the treatment of neck pain.
Eligibility Criteria
Inclusion
- Patients with chronic neck pain: post-whiplash injury, myofacial pain, cervical facet joint disease and idiopathic chronic neck pain
Exclusion
- Radiculopathy
- Myelopathy
- Cerebral vascular disease
- Malignancy
- Osteoporosis
- Cervical disc herniation
Key Trial Info
Start Date :
December 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 1 2011
Estimated Enrollment :
10 Patients enrolled
Trial Details
Trial ID
NCT01216566
Start Date
December 1 2010
End Date
May 1 2011
Last Update
October 7 2010
Active Locations (1)
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1
Hillel Yaffe Medical Center
Hadera, Israel, 38100