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Ultrasound Guided Diagnostic Cervical Medial Branch Block

This study has suspended participant recruitment.
(The PI has been unable to continue with the study.)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00896688
First Posted: May 12, 2009
Last Update Posted: September 7, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
McMaster University
Information provided by (Responsible Party):
McMaster University ( Hamilton Health Sciences Corporation )
April 30, 2009
May 12, 2009
September 7, 2017
January 2018
December 2019   (Final data collection date for primary outcome measure)
To determine the efficacy of the use of ultrasound for diagnostic cervical medial branch block on pain patients who have developed neck pain, cervicogenic headache, or shoulder pain. [ Time Frame: At time of procedure ]
Same as current
Complete list of historical versions of study NCT00896688 on ClinicalTrials.gov Archive Site
Interventional pain procedure studies on chronic pain patients [ Time Frame: At time of procedure ]
Same as current
Not Provided
Not Provided
 
Ultrasound Guided Diagnostic Cervical Medial Branch Block
Ultrasound Guided Diagnostic Cervical Medial Branch Block
The diagnostic cervical branch block for neck pain due to cervical facet joint pain has been traditionally done under fluoroscopic guidance. Its diagnostic value and technique have been well established. However, recently some studies have shown that the diagnostic cervical and lumbar medial branch block can be done under ultrasound guidance.
Not Provided
Observational
Observational Model: Other
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample
Primary care clinic
  • Facet Joint Pain
  • Neck Pain
Procedure: cervical medial branch blocks using the Quincke spinal needle
#25 gauge 1 and 1/2 inch long needle and #25 gauge 10cm long Quincke spinal needle will be used for placement.
  • Healthy Volunteers
    It will involve 5 volunteers and they will undergo C arm fluoroscopic guided cervical medial branch blocks (C2-C7) on unilateral position and then followed by the 3D ultrasound machine for visualization of needle position.
    Intervention: Procedure: cervical medial branch blocks using the Quincke spinal needle
  • Candidates for upper and lower cervial medical branch blocks
    This will involve 25 patients and they will follow the same procedures as the healthy volunteers.
    Intervention: Procedure: cervical medial branch blocks using the Quincke spinal needle

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Suspended
25
May 2020
December 2019   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • healthy volunteers
  • patients who have headache, neck pain, and shoulder pain due to possible facet joint disease

Exclusion Criteria:

  • patients/volunteers with BMI > 35
  • patients/volunteers with short thick neck
  • coagulopathy
  • allergy to local anesthetic, ultrasound gel
  • patient unable to fill out post procedure pain diary
Sexes Eligible for Study: All
18 Years to 65 Years   (Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
Canada
 
 
NCT00896688
08-575-D
No
Not Provided
Not Provided
McMaster University ( Hamilton Health Sciences Corporation )
Hamilton Health Sciences Corporation
McMaster University
Principal Investigator: Joseph Park, MD Hamilton Health Sciences Corporation
McMaster University
September 2017