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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00649753
Other study ID # SR0225080125
Secondary ID
Status Completed
Phase N/A
First received March 27, 2008
Last updated July 22, 2009
Start date March 2008
Est. completion date August 2008

Study information

Verified date March 2008
Source Logan College of Chiropractic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the relationship of pelvic blocking and protocol for cranial adjusting with specific pain areas as outlined by Dr. Bertrand DeJarnette in the Category II/sacroiliac protocol. An algometer will be used to determine the level of pain at specific points before and after each treatment of pelvic blocking with or without cranial adjusting.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date August 2008
Est. primary completion date August 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Logan student, staff or faculty

- Age 18 - 60

- No chiropractic adjustment 2 weeks prior to beginning the study

- Show the DeJarnette Category II indicators

Exclusion Criteria:

- Previous lower extremity, first rib and spine injury, surgery

- Local infection, injury or other malignancy affecting the lower extremity and the nervous system

- Unstable joints of the lower extremity and/or first rib and/or spine

- Prescription or herbal muscle stimulants, relaxants, etc. that could affect the nervous system

- Contraindication to DeJarnette Category II Pelvis Blocking

- Pregnancy

- Significant lower lumbar involvement

- Diabetes, shortness of breath on light physical activity, cardiovascular disease

- Numbness and/or tingling in the lower extremities

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Category II Pelvic Blocking
Supine Orthopedic Blocking consists of placing padded wedges underneath the Ilium and greater trochanter to correct pelvic torsion and associated sacroiliac dysfunction.
Category II Pelvic Blocking and Cranial
Supine Orthopedic Blocking consists of placing padded wedges underneath the Ilium and greater trochanter to correct pelvic torsion and associated sacroiliac dysfunction. During pelvic blocking a cranial procedure is performed using a zygomae release and sphenobasilar release. These cranial procedures are manual therapy procedures using light pressure from hand and/or finger contacts.
Cranial Only
Without pelvic blocking a cranial procedure is performed using a zygomae release and sphenobasilar release. These cranial procedures are manual therapy procedures using light pressure from hand and/or finger contacts.

Locations

Country Name City State
United States Logan University, College of Chiropractic Chesterfield Missouri

Sponsors (1)

Lead Sponsor Collaborator
Logan College of Chiropractic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Algometer readings pre and post treatment intervention No
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