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Comparison of the ProAdjuster Analysis to the Penning Method of Determining Intersegmental Motion of the Cervical Spine

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00321529
First Posted: May 3, 2006
Last Update Posted: May 24, 2007
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.
Information provided by:
Logan College of Chiropractic
  Purpose
The purpose of this study is to determine if the ProAdjuster system of analysis can be used to determine cervical spine instability using the Penning system of radiographic marking as a standard of comparison.

Condition Intervention
Cervical Spine Instability Device: motion analysis by durometer

Study Type: Observational
Study Design: Observational Model: Defined Population
Primary Purpose: Screening
Time Perspective: Longitudinal
Time Perspective: Retrospective

Resource links provided by NLM:


Further study details as provided by Logan College of Chiropractic:

Study Completion Date: October 2006
Detailed Description:
This study will utilize the ProAdjuster Device as a method of assessing the motion of the cervical spine in participants with instability as determined by a Penning Radiographic analysis. Only participants with existing radiographic studies will be included in the study. No additional Radiographic will be required.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   20 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria: Logan student, staff, or faculty with no history of ankle injury; 2. Age 18 – 60 yoa.

Exclusion Criteria: 1. Logan student, staff, or faculty ; 2. Local infection, injury or other malignancy affecting the cervical spine; 3. Any unstable joints of the cervical spine than require immobilization ; 4. Any manipulation to cervical spine within 48 hours; 5. Pregnancy.

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00321529


Locations
United States, Missouri
Logan College of Chiropractic
Chesterfield, Missouri, United States, 63017
Sponsors and Collaborators
Logan College of Chiropractic
Investigators
Principal Investigator: Dennis E. Enix, DC Logan Chiropractic College
  More Information

ClinicalTrials.gov Identifier: NCT00321529     History of Changes
Other Study ID Numbers: 0327060002
First Submitted: May 1, 2006
First Posted: May 3, 2006
Last Update Posted: May 24, 2007
Last Verified: May 2007

Keywords provided by Logan College of Chiropractic:
Cervical spine instability
Penning Study