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Clinical Trials/NCT01216566
NCT01216566
Unknown
Phase 1

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

Hillel Yaffe Medical Center1 site in 1 country10 target enrollmentDecember 2010
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.

Registry
clinicaltrials.gov
Start Date
December 2010
End Date
May 2011
Last Updated
15 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

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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