Evaluating the Effect of Acupuncture on Pain Relief Using Quantitative Sensory Testing (QST)



Status:Active, not recruiting
Conditions:Chronic Pain
Therapuetic Areas:Musculoskeletal
Healthy:No
Age Range:18 - 65
Updated:7/4/2018
Start Date:January 2010
End Date:December 2018

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Evaluating the Effect of Acupuncture on Pain Relief Using QST

The purpose of this study is to explore a new approach in assessing the effectiveness of
acupuncture therapy in the treatment chronic pain conditions.


Inclusion Criteria:

1. Subject will be between ages 18 to 65 years. Both male and female subjects will be
recruited.

2. Subject should have had cervical or lumbar radicular pain for at least two months.
This requirement is to avoid the uncertainty of an unstable pain condition and to
minimize the study variation.

3. Subject has a pain score of 4 or above (Visual Analog Scale (VAS): 0 - 10 from no pain
to worst pain).

4. Cervical or lumbar radicular pain will include, but is not limited to, such clinical
conditions as disk herniation, spinal stenosis, and post-laminectomy syndrome.

5. For controls, healthy subjects without radicular pain for at least three months will
be recruited. *We are no longer accepting healthy volunteers.*

Exclusion Criteria:

1. Subject has detectable sensory deficits at the site of QST. Sensory deficits refer to
such conditions resulting from neurological diseases or medical conditions causing
peripheral polyneuropathy and sensory changes, which include but are not limited to
diabetic neuropathy, alcoholic neuropathy, AIDS neuropathy, severe thyroid disease,
and severe liver or kidney disorders.

2. Subject has scar tissue, infection, or acute injury at the site of QST.

3. Subject is on anticoagulation therapy.

4. Subject is pregnant.

5. Subject is tested positive on illicit drugs.
We found this trial at
1
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Boston, Massachusetts 02114
Phone: 617-724-6102
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