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

NCT ID: NCT01216566

Last Updated: 2010-10-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE1/PHASE2

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-12-31

Study Completion Date

2011-05-31

Brief Summary

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

Detailed Description

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Conditions

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Neck Pain

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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I. Patients with chronic neck pain

Group Type EXPERIMENTAL

Occiflex Device

Intervention Type 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

Interventions

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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

Intervention Type DEVICE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Headway Ltd.

UNKNOWN

Sponsor Role collaborator

Hillel Yaffe Medical Center

OTHER_GOV

Sponsor Role lead

Responsible Party

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Dept. of Neurology, Hillel Yaffe Medical Center

Locations

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Hillel Yaffe Medical Center

Hadera, , Israel

Site Status

Countries

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Israel

Facility Contacts

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Yaron M River, MD

Role: primary

[email protected]
972-4-6304427

Other Identifiers

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HYMC-0030-10

Identifier Type: -

Identifier Source: org_study_id