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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00562562
Other study ID # 15148
Secondary ID 15148
Status Completed
Phase N/A
First received November 21, 2007
Last updated April 19, 2017
Start date September 2007
Est. completion date December 2008

Study information

Verified date April 2017
Source Ohio University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a pilot project intended to determine the feasibility of detecting soft tissue changes in response to osteopathic manipulative treatment (OMT). MRIs of the lumbar and pelvic regions of low back pain (LBP) patients will be taken once before and at two different time points after OMT. Images obtained will be quantitatively analyzed for changes in the volumes of back muscles and for changes (T2 signals) indicative of activity levels or pathological conditions. Electromyography (EMG) will be used as an independent measure of back muscle activity for comparison with MRI results.


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion criteria:

- Adult patients (18-55)

- Patients with LBP with acute symptoms (within last 3 weeks)

- Test positive for lumbar somatic dysfunction

Exclusion criteria:

- History of any spinal injuries/surgeries

- Positive findings of frank neurological signs during physical exam

- Any other orthopedic or neurological impairment

- Unsuitable for MRI imaging:

- Cardiac pacemaker or defibrillator

- Severe Claustrophobia

- Injured by a metallic object that was not removed

- Cochlear (ear) implants

- Surgery involving a metallic implant (e.g. knee replacement)

- Weight more than 300 lbs/136 kg (weight limit for scanner bed)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
osteopathic manipulative treatment
Treatment will focus on the thoracolumbar junction, L5, the sacrum, and the pubes. Treatment will primarily utilize two techniques, muscle energy and ligamentous-articular release, but will be tailored to the findings of the individual patient.

Locations

Country Name City State
United States Ohio University Athens Ohio

Sponsors (2)

Lead Sponsor Collaborator
Ohio University Osteopathic Heritage Foundations

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary MRI T2 signal changes within 72 hours
Secondary MRI anatomic changes and EMG changes within 72 hours
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