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Algometer and Category II Pelvic Blocking and Cranial Protocol — Algometer  

Pain Clinical Trial

Official title:
An Investigation of Algometer Readings for DeJarnette Category II Indicators After Category II Blocking and Cranial Protocol

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.

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00649753
Study type Interventional
Source Logan College of Chiropractic
Contact
Status Completed
Phase N/A
Start date March 2008
Completion date August 2008
View Details
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