Computerized Mobilization of the Cervical Spine Utilizing the Occiflex Device for the Treatment of Chronic Neck Pain
Unknown statusPhase 1, Phase 2NCT01216566
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The purpose of this study is to investigate the efficacy and safety of the Occiflex device in the treatment of neck pain.
Study details
- Conditions
- Interventions
- Device: Occiflex Device
- Sponsor
- Hillel Yaffe Medical Center
- Collaborators
- Headway Ltd.
- Start date
- 2010-12
- Primary completion
- 2011-04
- Sex
- All
- Age range
- from 18 Years to 65 Years
- Results posted
- No results posted in this snapshot
- Countries
- Israel
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
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
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01216566