Analgesic Effect of Accelerated Repetitive Transcranial Magnetic Stimulation in Pain Related to Peripheral Neuropathy
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Peripheral Neuropathy
- Sponsor
- Jakub Antczak
- Enrollment
- 70
- Locations
- 1
- Primary Endpoint
- Visual Analogue Scale of Pain Severity after rTMS
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
Peripheral neuropathy is a frequent condition, commonly associated with pain. Repetitive Transcranial Magnetic Stimulation (rTMS) is a noninvasive method of modulation of brain plasticity and is regarded as one of alternative methods to alleviate pain associated with various kind of neuropathies. rTMS is usually performed once a day and the whole therapy of neuropathic pain lasts one week. In a number of recent clinical trials including patients with depression and some other disorders, rTMS was delivered several times a day, which reduced the time of the whole therapy. This approach was termed an accelerated rTMS. The purpose of this study is to investigate feasibility of accelerated rTMS in treatment of neuropathic pain.
Detailed Description
Peripheral neuropathy is a frequent condition, commonly associated with pain, which is often drug resistant. Repetitive Transcranial Magnetic Stimulation (rTMS) is a noninvasive method of modulation of brain plasticity. In this method, series of magnetic stimuli are delivered to the cerebral cortex, where they turn to electric current and depolarize repetitively the targeted neurons. If the stimulation is repeated during subsequent days it is capable to modify the activity of targeted cortical area for weeks or even months and by this way to achieve therapeutic effect. rTMS is most commonly used to treat drug-resistant depression but a number of other psychiatric and neurologic conditions is increasingly being regarded as therapeutic indication for rTMS. In patients suffering from neuropathic pain rTMS is delivered with high frequency, over primary motor areas (PMA). Stimulation of PMA should result in modulation of thalamic activity, achieved by antidromic excitation of thalamocortical connections. rTMS is usually performed once a day and the whole therapy of neuropathic pain lasts one week. In a number of recent clinical trials including patients with depression and some other disorders, rTMS was delivered several times a day, which reduced the time of the whole therapy. This approach was termed an accelerated rTMS. The purpose of this study is to investigate feasibility of accelerated rTMS in treatment of neuropathic pain.
Investigators
Jakub Antczak
Principal Investigator
Jagiellonian University
Eligibility Criteria
Inclusion Criteria
- •Diagnosis of peripheral neuropathy
- •Neuropathic pain of constant severity since not less than a month and requiring use of analgesics more than once a week
- •Score of 30 millimeter or more on the 100 millimeter visual analog scale of pain intensity at inclusion
Exclusion Criteria
- •Severe depression
- •Personality disorders and other psychiatric conditions, which could disturb the participation in the study
- •Cognitive deficits, which could disturb the participation in the study
- •Presence of magnetic material in the reach of magnetic field
- •Pregnancy
- •Likelihood to get pregnant
- •Intracranial electrodes
Outcomes
Primary Outcomes
Visual Analogue Scale of Pain Severity after rTMS
Time Frame: Through study completion, an average of 1 year.
An analog scale of the length of 100 millimeter. Total score of 100, with higher scores representing more severe pain. Change from baseline score in the Visual Analogue Scale to the measurement taken after finishing rTMS.
Visual Analogue Scale of Pain Severity First Follow-up
Time Frame: Before rTMS, up to one day after finishing rTMS.
An analog scale of the length of 100 millimeter. Total score of 100, with higher scores representing more severe pain. Change from baseline score in the Visual Analogue Scale to the measurement taken after two weeks after finishing rTMS.
Visual Analogue Scale of Pain Severity Second Follow-up
Time Frame: Before rTMS, four weeks after finishing rTMS.
An analog scale of the length of 100 millimeter. Total score of 100, with higher scores representing more severe pain. Change from baseline score in the Visual Analogue Scale to the measurement taken after four weeks after finishing rTMS.
Secondary Outcomes
- Numeric Pain Severity Scale after rTMS(Before rTMS, up to one day after finishing rTMS.)
- Numeric Pain Severity Scale First Follow-up(Before rTMS, two weeks after finishing rTMS.)
- Numeric Pain Severity Scale Second Follow-up(Before rTMS, four weeks after finishing rTMS.)
- Neuropathic Pain Symptoms Inventory after rTMS(Before rTMS, up to one day after finishing rTMS.)
- Neuropathic Pain Symptoms Inventory First Follow-up(Before rTMS, two weeks after finishing rTMS.)
- Neuropathic Pain Symptoms Inventory Second Follow-up(Before rTMS, four weeks after finishing rTMS.)
- Athens Insomnia Scale after rTMS(Before rTMS, up to one day after finishing rTMS.)
- Athens Insomnia Scale First Follow-up(Before rTMS, two weeks after finishing rTMS.)
- Athens Insomnia Scale Second Follow-up(Before rTMS, four weeks after finishing rTMS.)
- Bilateral Dynamometric Assessment of the strength of the foot extension after rTMS(Before rTMS, up to one day after finishing rTMS.)
- Bilateral Dynamometric Assessment of the strength of the foot extension First Follow-up(Before rTMS, two weeks after finishing rTMS.)
- Bilateral Dynamometric Assessment of the strength of the foot extension Second Follow-up(Before rTMS, four weeks after finishing rTMS.)