Phase 2
Completed N=10
Tailored Computerized Mobilization of the Cervical Spine Utilizing the Occiflex Device for the Treatment of Chronic Neck Pain
Source: ClinicalTrials.gov NCT01518530 ↗Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Oct 2013
Primary outcomePrimary: Occiflex Device Safety — 26 Number of adverse effects
Summary
The study is intended to examine the safety and efficacy of computerized mobilization of the neck for the treatment of patients with chronic neck pain. This is a third continuation study aimed at examining the Occiflex Robotic System. This time we will be studying tailored or personalized three dimensional movement of the neck.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Occiflex Device Safety |
26 | — |
| SECONDARY Efficacy as Per the NDI-Neck Disability Index |
— | — |
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
- Patients with cervical radiculopathy Myelopathy Discopathy Malignancy involving the neck or cervical spine Severe Osteoporosis Severe skin disorder Psychiatric disorders Cervical disc herniation
Data sourced from ClinicalTrials.gov (NCT01518530). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.