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NCT01216566 Clinical Trial

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

Neck Pain Clinical Trial

Clinical Trial Details — Status: Unknown status

Administrative data
NCT number NCT01216566
Other study ID # HYMC-0030-10
Secondary ID
Status Unknown status
Phase Phase 1/Phase 2
First received June 1, 2010
Last updated October 6, 2010
Start date December 2010
Est. completion date May 2011

Study information
Verified date October 2010
Source Hillel Yaffe Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Unknown status
Enrollment 10
Est. completion date May 2011
Est. primary completion date April 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Occiflex Device
This device is a computerized robotic platform that allows continuous mobilization of the cervical spine in a three dimensional space. The patients undergoes biweekly 20 minute therapeutic session for 6 weeks

Locations
Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (2)
Lead Sponsor Collaborator
Hillel Yaffe Medical Center Headway Ltd.

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Safety of computerized continuous mobilization of the cervical spine one year
Secondary Efficacy of computerized mobilization of treatment of patients with chronic neck pain one year
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