Status:

COMPLETED

Botulinum Toxin Injection in Neck Muscles in Cervicogenic Headache

Lead Sponsor:

Norwegian University of Science and Technology

Conditions:

Cervicogenic Headache

Eligibility:

All Genders

18-70 years

Phase:

PHASE2

Brief Summary

The purpose of this study is to investigate the effect and side-effects of injections with botulinum toxin in neck muscles in cervicogenic headache compared to injections with sodium water.

Detailed Description

Cervicogenic headache is a unilateral headache stemming from the neck. Usually, there are no pathological findings on x-ray or MRI of the neck. It is supposed that pain may stem from various structure...

Eligibility Criteria

Inclusion

  • Headache strictly unilateral without side-shift
  • Traits indicating involvement of neck structures, fulfilling at least 2 of the following:
  • I. Reduced neck range of motion II. Typical headache can be elicited by palpation or pressure on muscles of the occiput or in the neck.
  • III. Typical headache can be precipitated by certain neck movements or by adopting a certain position of the head.
  • IV. There is a radiation of pain to the ipsilateral shoulder or arm.
  • Positive effect of blockades. (In this study only a blockade of the greater occipital nerve will be applied).
  • The condition has lasted for more than 1 year.
  • The headache should be present more than 15 days a month, and the frequency should be based on a headache diary filled in the last month before inclusion.

Exclusion

  • Cervical spinal stenosis, cervical disc herniation, or other neck pathology that should be treated surgically.
  • Malignant disorder.
  • Rheumatic disorder or other disorders which induces analgesic use.
  • other clinically relevant disease (liver, kidney, endocrinological, metabolical, systemic, psychiatric).
  • Frequent other headache type that cannot be distinguished from cervicogenic headache.
  • Pending or ongoing litigation for head- or neck trauma.

Key Trial Info

Start Date :

May 1 2005

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2009

Estimated Enrollment :

28 Patients enrolled

Trial Details

Trial ID

NCT00184197

Start Date

May 1 2005

End Date

December 1 2009

Last Update

March 13 2017

Active Locations (1)

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1

Dept. of Neurology and Clinical Neurophysiology, Norwegian Headache Centre

Trondheim, Norway, 7006