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

Phase 1

• Conditions: Neck Pain
• Interventions: Device: Occiflex Device

• Registration Number: NCT01216566
• Lead Sponsor: Hillel Yaffe Medical Center

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2010-06-01
• Status Verified: 2010-10
• Study First Submitted QC: 2010-10-06
• Last Update Submitted: 2010-10-06
• Study First Posted: 2010-10-07
• Last Update Posted: 2010-10-07
• Study Start: 2010-12
• Primary Completion: 2011-04
• Study Completion: 2011-05

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 10

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

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
I. Patients with chronic neck pain	Occiflex Device	-

Primary Outcome Measures

Name	Time	Method
Safety of computerized continuous mobilization of the cervical spine	one year

Secondary Outcome Measures

Name	Time	Method
Efficacy of computerized mobilization of treatment of patients with chronic neck pain	one year

Trial Locations

Locations (1)

Hillel Yaffe Medical Center; 🇮🇱 Hadera, Israel