Movement Disorder Clinical Trial
Official title:
Treatment of Cortical Myoclonus With Repetitive Transcranial Magnetic Stimulation
Myoclonus is a condition related to epilepsy of involuntary twitching or jerking of the
limbs.
The purpose of this study is to determine if stimulation of the brain with magnetic pulses
can decrease myoclonus. Researchers believe that this may be possible because in studies on
normal volunteers, magnetic stimulation made areas of the brain difficult to activate for
several minutes. In addition, early studies on patients with myoclonus have shown magnetic
stimulation to be effective at decreasing involuntary movements.
Transcranial Magnetic Stimulation (TMS) is a non-invasive technique that can be used to
stimulate brain activity and gather information about brain function. It is very useful when
studying the areas of the brain and spinal cord related to motor activity (motor cortex and
corticospinal tract). Repetitive transcranial magnetic stimulation (rTMS) involves the
placement of coil of wire (electromagnet) on the patient's scalp and rapidly turning on and
off the electrical current. The changing magnetic field produces weak electrical currents in
the brain near the coil. This permits non-invasive, relatively localized stimulation of the
surface of the brain (cerebral cortex). The effect of magnetic stimulation varies, depending
upon the location, intensity and frequency of the magnetic pulses.
Researchers plan to use rTMS for 10 days on patients participating in the study. The 10 day
period will be broken into 5 days of active repetitive magnetic stimulation and 5 days of
placebo "ineffective" stimulation. At the end of the 10 day period, if the results show that
rTMS was beneficial, patients may undergo an additional 5 days of active rTMS.
Status | Completed |
Enrollment | 10 |
Est. completion date | January 2002 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Age 5 to 90 with severe cortical myoclonus. No intracranial metal hardware (excluding dental fillings), pacemakers, indwelling medication pumps, cochlear implants, intracardiac lines, significant intracranial masses or increased intracranial pressure. Subject must not be pregnant. |
Endpoint Classification: Safety Study, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | National Institute of Neurological Disorders and Stroke (NINDS) | Bethesda | Maryland |
Lead Sponsor | Collaborator |
---|---|
National Institute of Neurological Disorders and Stroke (NINDS) |
United States,
Cantello R, Gianelli M, Civardi C, Mutani R. Magnetic brain stimulation: the silent period after the motor evoked potential. Neurology. 1992 Oct;42(10):1951-9. — View Citation
Fuhr P, Agostino R, Hallett M. Spinal motor neuron excitability during the silent period after cortical stimulation. Electroencephalogr Clin Neurophysiol. 1991 Aug;81(4):257-62. — View Citation
Inghilleri M, Berardelli A, Cruccu G, Manfredi M. Silent period evoked by transcranial stimulation of the human cortex and cervicomedullary junction. J Physiol. 1993 Jul;466:521-34. — View Citation
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