Clonidine-induced Spinal Acetylcholine Release: Normal Volunteers vs. Neuropathic Pain



Status:Completed
Conditions:Chronic Pain
Therapuetic Areas:Musculoskeletal
Healthy:No
Age Range:18 - Any
Updated:9/12/2018
Start Date:September 2004
End Date:March 2008

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The purpose of this study is to compare the amount of acetylcholine release after a single
injection of clonidine in normal volunteers and individuals with neuropathic pain.

This study is part of a pain center grant that focuses on how pain, especially chronic
neuropathic pain, alters the response to traditional and non-traditional analgesics (pain
medications).

The way that nerve fibers carry pain information to the brain is thought to change after
surgery and in cases of chronic pain. For this reason, some medicines work better to relieve
pain in healthy people who have a sudden painful injury when compared to people after surgery
or to people with chronic pain. Currently available pain medications may not relieve all
types of pain or may relieve pain only at doses that produce side effects and potential
complications.

The aim of this study is to understand the mechanisms by which intrathecal clonidine (or
clonidine injected into cerebrospinal fluid) increases in potency and efficacy by examining
the cerebrospinal fluid of healthy individuals, before and after clonidine administration, as
well as looking at the spinal fluid of people with chronic neuropathic nerve pain. More
specifically, in this study, researchers will compare acetylcholine release (a protein-like
substance found in cerebrospinal fluid) in normal volunteers and patients with neuropathic
pain after a single injection of clonidine.

After baseline measurements, including blood pressure and heart rate, participants will be
trained to accurately estimate pain by way of thermal heat testing. Next a small amount of
spinal fluid will be withdrawn from each participant to measure the amounts of naturally-made
chemicals in the participants' cerebrospinal fluid. Participants then will receive an
injection of clonidine. After the injection, additional samples of spinal fluid will be taken
to measure chemical changes in the fluid.

Duration of the study for participants is 1 day, and includes 1 visit to the research center,
lasting approximately 3 hours.

Inclusion Criteria:

- Healthy adult volunteers

- Patients with neuropathic pain

Exclusion Criteria:

- Pregnancy

- Allergy to clonidine

- Currently taking clonidine or other direct a2-adrenergic agonists

- Taking cholinesterase inhibitors
We found this trial at
2
sites
145 Kimel Park Drive
Winston-Salem, North Carolina 27103
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