Pain Clinical Trial
Official title:
The Effect of 10-Day Treatment of Repetitive Transcranial Magnetic Stimulation on Abdominal Pain in Patients With Chronic Pancreatitis
The researchers aim to study the effects of repetitive transcranial magnetic stimulation (rTMS) on chronic visceral pain in patients with idiopathic chronic pancreatitis.
The purpose of this protocol is to investigate a possible novel treatment for intractable
visceral pain in patients with chronic pancreatitis. Pain is a major contributor to the poor
quality of life in patients with chronic pancreatitis. The refractory nature of this
condition to medical and surgical procedures prompted us to hypothesize that one mechanism
leading to pain in these patients is the dysfunction of brain cortical regulation of visceral
sensation. This notion is particularly supported by findings that patients with chronic
pancreatitis can continue to experience disabling pain even after total pancreatectomy. This
suggests that symptoms are sustained by a pancreas-independent, neural-based mechanism.
Visceral sensation is particularly processed in the secondary somatosensory area - SII.
Therefore, chronic pancreatitis pain may be sustained by a dysfunction of SII rather than by
pancreatic inflammation alone. The researchers hypothesize further that the dysfunction of
SII is one of hyper-excitability. According to this hypothesis, suppression of SII activity
may help control the pain in patients with chronic pancreatitis. Temporary inhibition of SII
activity can be obtained by a novel tool, namely transcranial magnetic stimulation (TMS),
which can suppress brain excitability non-invasively beyond the duration of the TMS if
appropriate stimulation parameters are employed. In the initial sham controlled, double blind
pilot trial of 5 subjects with idiopathic chronic pancreatitis, TMS applied to SII resulted
in significant pain improvement in 3 of the subjects. The researchers will rigorously test
the hypothesis that chronic pancreatitis pain is sustained by a dysfunction of SII
characterized by hyperexcitability through two specific aims:
1. The first aim of this study is to examine whether slow repetitive TMS (rTMS) applied to
SII in patients with pain and chronic pancreatitis has an analgesic effect as measured
by changes in the Visual Analogue Scale (VAS) for pain and a decrease in analgesic
intake, as well as an overall improvement in quality of life. In addition, if this study
finds a significant effect of rTMS on pain reduction, the duration of this effect will
be further assessed. TMS will be applied at parameters of stimulation known to decrease
excitability.
2. The second aim of the study is to assess the safety of rTMS in this patient population.
In the pilot study none of the patients experienced any adverse effects of a single
session of rTMS. However, the extension of the study protocol to a 10-day course of
daily rTMS requires careful safety assessment. Fifteen-day courses of rTMS have been
used for treatment of various neuropsychiatric diseases without any complications if
safety guidelines are carefully followed. The researchers will adhere to the current
safety recommendations for rTMS endorsed by the International Society for Transcranial
Stimulation and the International Federation for Clinical Neurophysiology. Therefore,
the researchers hypothesize that the proposed rTMS protocol will be safe for the patient
population.
3. The third aim of the study is to study the physiologic mechanism of action of rTMS in
these patients using magnetic resonance imaging (MRI). In doing so, the researchers aim
to contribute to a better understanding of the pathophysiology of chronic pain in
patients with pancreatitis by investigating the correlation between pain improvement and
areas of brain activation. This could lead to the development of markers of therapeutic
response. Magnetic resonance spectroscopy allows a non-invasive measure of GABAergic and
glutamatergic activity in a defined volume of interest in the brain. The researchers
hypothesize that the balance of GABA and glutamate will be abnormal in SII in patients
with pain from chronic pancreatitis, with a relative decrease in GABA and increase in
glutamate indicating an abnormal, hyperexcitable dysfunction. This abnormality will be
normalized by rTMS in correlation with its analgesic effect.
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