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Cervical Spine InstabilityNCT00321529

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

An observational study of Cervical Spine Instability, run by Logan College of Chiropractic at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 20 to 60 yearsHealthy volunteers can take part
Conditions the study is for
Cervical Spine Instability
What is being tested?
motion analysis by durometer
Type of treatment
Medical device
How many people
Not given
Where
1 siteUnited States
Study dates
Start not givento Oct 2006
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 60 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

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.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Logan College of Chiropractic

    Chesterfield, Missouri, 63017

Other trials in United States

About this study

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.

Read the 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.

Being tested
motion analysis by durometer
Keywords
Cervical spine instability, Penning Study

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • motion analysis by durometerDevice

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 May 2006 (estimated)
  2. Study completionOct 2006

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Defined population
Time perspective
Retrospective
IDs, dates and publications
ClinicalTrials.gov ID
NCT00321529
Sponsor's protocol ID
0327060002
Status last verified
May 2007
First submitted
1 May 2006
Last updated
24 May 2007
Results posted
No

Questions about this trial

What is this clinical trial studying?

An observational study of Cervical Spine Instability, run by Logan College of Chiropractic at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 May 2007. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 May 2007.

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