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

Hillel Yaffe Medical Center

Status and phase: Unknown; Phase 2; Phase 1

Conditions: Neck Pain

Treatments: Device: Occiflex Device

Study type: Interventional

Funder types: Other

Identifiers

NCT01216566

HYMC-0030-10

Details and patient eligibility

About

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

Enrollment: 10 estimated patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

---

10 participants in 1 patient group

I. Patients with chronic neck pain

Experimental group

Treatment:

Device: Occiflex Device