Neuropathic pain (NP) is one type of refractory chronic pain condition,medical treatments for NP is limited because of its poorly response. A noninvasive brain-stimulation method called transcranial magnetic stimulation (TMS) has garnered interest as an alternative treatment for intractable NP potentially through inducing therapeutic brain plasticity.Indeed, high-frequency (≥ 5 Hz) Repetitive TMS (rTMS) over the primary motor cortex (M1) is suggested to be able to reduce neuropathic pain in randomized controlled studies.Overall, the clinical application of rTMS in chronic pain is still limited by the response rate,the investigation of rTMS protocols is important for improving rTMS analgesia. Theta burst stimulation (TBS) mimics the bursts of neuronal firing which results in robust long-term potentiation. Continuous TBS (cTBS) is designed to decrease excitability, whereby prolonged cTBS (pcTBS, i.e. multiple cTBS being delivered continuously) has recently been demonstrated to increase excitability. More importantly, pcTBS was found to have comparable or even better analgesic effects than standard 10 Hz rTMS. These findings together call for more studies to validate the analgesic efficacy of pcTBS. In this study, the investigators aim to assess and compare the efficacy of prolonged continuous theta burst stimulation (pcTBS) with 10HZ rTMS in NP patients.
The investigators designed a randomized, double-blind, sham-controlled study at 1 center. fifty NP patients were randomly assigned to 3 groups. A series of 5 daily pcTBS(1200 pulses/session) or 10-Hz rTMS (1500 pulses/session) of primary motor cortex (M1) or sham stimulation was applied to each patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
94
Participants received 10HZ rTMS protocol consisted of 5 sessions over 5 consecutive workdays
Participants received pcTBS protocol consisted of 5 sessions over 5 consecutive workdays
Participants received Sham rTMS stimulations consisted of 5 sessions over 5 consecutive workdays
The second affiliated hospital of Zhejiang University hangzhou
Hangzhou, Zhejiang, China
The mean change from baseline in pain intensity measured with the visual-analogic scale (VAS)
The primary outcome measure was the mean change from baseline over the course of 5 (group by time interaction) in average pain intensity measured with the visual-analogic scale (VAS) ( 0= no pain and 10= maximal pain). Baseline average pain intensity was assessed at inclusion then on the day of randomization, just before the first rTMS session (day 1) and corresponded to the average of these two values.
Time frame: through study completion, an average of 8 months
Motor-evoked potential (MEP)
Corticospinal excitability was measured with MEP at rest of the first dorsal interosseous (FDI) muscle, A total of 20 single pulses were consecutively delivered to the hand region of the left M1 at 120% RMT (45° to the midline, handle pointing backward).
Time frame: through study completion, an average of 8 months
Cortical silent period (CSP)
Corticospinal excitability was measured with CSP during a sustained voluntary FDI muscle contraction, A total of 20 single pulses were consecutively delivered to the hand region of the left M1 at 120% RMT (45° to the midline, handle pointing backward).
Time frame: through study completion, an average of 8 months
The sensory dimension of pain and affective dimension of pain
The sensory dimension of pain (rated on 33) and affective dimension of pain (rated on 12) from the 15-items Short form of the McGill Pain questionnaire (SF-MPQ) .
Time frame: through study completion, an average of 8 months
Pain interference scale
7 items rated from 0= does not interfere to 10= complete interference, total score 70 from the Brief Pain Inventory.
Time frame: through study completion, an average of 8 months
Patients global impression of change
the 7 items Patients global impression of change (PGIC) (from very much worse to very much improved)
Time frame: through study completion, an average of 8 months
The depression score
ranging from 0 to 13 with higher scores indicating more severe depression from the 13 items Beck Depression Inventory (BDI)
Time frame: through study completion, an average of 8 months
release of neurotransmitters
Measured with magnetic resonance spectroscopy,MRS
Time frame: through study completion, an average of 8 months
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