Transcranial Magnetic Stimulation (TMS) Effects on Pain Perception

Medical University of South Carolina (MUSC)

Status and phase

Withdrawn

Phase 3

Phase 2

Conditions

Neuropathic Pain

Trigeminal Neuralgia

Pain

Treatments

Device: laboratory pain assessment

Procedure: transcranial magnetic stimulation

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT00349050

K23NS050485-01A2 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to investigate the effects of transcranial magnetic stimulation on pain perception.

Full description

Chronic pain represents a huge public health concern and is generally poorly understood at a basic neurobiological level. Transcranial magnetic stimulation (TMS) is a non-invasive technique that uses electromagnetic pulses to temporarily stimulate specific brain areas in awake people (without the need for surgery, anesthesia, or other invasive procedures). Previous research suggests that TMS may be effective in reducing pain perception in healthy adults and in patients with various types of pain conditions, such as neuropathic pain. However, there is relatively little research on TMS and pain that addresses optimal TMS device parameters, optimal cortical targets, and potential differences in response to TMS between healthy persons and those with chronic pain.

The purpose of this trial is to study the effects of TMS on pain perception. Specifically, this study will determine optimal device parameters (dose) and brain targets for stimulation with TMS in order to reduce pain in patients with neuropathic pain and in healthy adults using laboratory pain methods.

Participants with Neuropathic Pain:

After an initial screening, eligible participants with neuropathic pain will receive a magnetic resonance imaging (MRI) scan to help determine the best target for TMS stimulation later in the study. Participants will be asked to record their pain experiences every day for 2-4 weeks before receiving the first of 2 laboratory pain assessments. The laboratory pain assessment uses a small device, controlled by a computer and attached to the underside of the forearm, to produce different temperature stimulations. As the device reaches a level considered painful to the participant, he/she can push a button to return to a level of comfort.

The next part of the trial involves two, 20-minute TMS treatment sessions per day for 5-days. Participants will be randomly assigned to one of two groups. Group A will receive real TMS and Group B will receive "sham" TMS. Study participation time for individuals with TGN is about 8 weeks, including about 10 hours (7 visits) at the Medical University of South Carolina (MUSC).

Healthy Volunteers:

In addition to an interview with researchers regarding medical history, healthy participants will complete a self-report screening to assess pain history and level of depression and anxiety. Eligible participants will be given a laboratory pain assessment, and be randomly assigned to one of two groups: group A will receive real TMS and group B will receive "sham" TMS. After TMS, participants will receive another full laboratory pain assessment and complete questionnaires. For healthy volunteers, participation in the study will take about 3 hours and may be completed in one or two visits.

Sex

All

Ages

21 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

For Healthy Adults:

Between age of 21 and 60
No prescription medications in previous 3 months
No seizure history
No depression
Not suicidal
No anxiety
No hospitalizations or surgeries in previous 6 months
No history of chronic pain conditions
No implanted metal devices (e.g., pacemakers, metal plates, wires)
Not pregnant
No alcohol abuse/dependence history in previous 6 months
No illicit drug use in previous 6 months
Capable of reading, writing, giving consent, following instructions
No history of brain surgery or history of loss of consciousness >15 minutes
No history of autoimmune or endocrine disorder
No significant anxiety about entering MRI scanner

For Patients with neuropathic pain:

Between age of 21 and 75
No seizure history
Not taking medications shown to increase seizure risk (6 months)
Not suicidal
No hospitalizations or surgeries in previous 3 months
No implanted metal devices (e.g., pacemakers, metal plates, wires)
Not pregnant
No alcohol abuse/dependence history in previous 6 months
No illicit drug use in previous 6 months
Capable of reading, writing, giving consent, following instructions
Chronic pain (>6 months), not significantly relieved by pharmacological treatment
No significant anxiety about entering MRI scanner